Item | Value |
---|---|
geneid | 25821 |
ensemblid | ENSG00000135297.17 |
hgncid | 19261 |
symbol | MTO1 |
name | mitochondrial tRNA translation optimization 1 |
refseq_nuc | NM_012123.4 |
refseq_prot | NP_036255.2 |
ensembl_nuc | ENST00000498286.6 |
ensembl_prot | ENSP00000419561.2 |
mane_status | MANE Select |
chr | chr6 |
start | 73461737 |
end | 73509236 |
strand | + |
ver | v1.2 |
region | chr6:73461737-73509236 |
region5000 | chr6:73456737-73514236 |
regionname0 | MTO1_chr6_73461737_73509236 |
regionname5000 | MTO1_chr6_73456737_73514236 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 692 | 391 | 87 | 72 | 183 | 18 | 29 | 141 | MTO1_chr6_73456737_73514236 | MTO1 | MFYFR others(687): Show |
chr6 | 73456737 | 73514236 |
a0002 | 0/0 | 692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | MFYFR others(687): Show |
chr6 | 73456737 | 73514236 |
a0003 | 0/0 | 692 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | MFYFR others(687): Show |
chr6 | 73456737 | 73514236 |
a0004 | 0/0 | 692 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | MFYFR others(687): Show |
chr6 | 73456737 | 73514236 |
a0005 | 0/0 | 692 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | MFYFR others(687): Show |
chr6 | 73456737 | 73514236 |
a0006 | 0/0 | 692 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | MFYFR others(687): Show |
chr6 | 73456737 | 73514236 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2076 | 308 | 66 | 59 | 142 | 15 | 25 | MTO1_chr6_73456737_73514236 | MTO1 | ATGTT others(2071): Show |
chr6 | 73456737 | 73514236 | ||
a0001c0002 | 0/0 | 2076 | 80 | 19 | 13 | 41 | 3 | 4 | MTO1_chr6_73456737_73514236 | MTO1 | ATGTT others(2071): Show |
chr6 | 73456737 | 73514236 | ||
a0001c0003 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | ATGTT others(2071): Show |
chr6 | 73456737 | 73514236 | ||
a0001c0007 | 0/1 | 2076 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | ATGTT others(2071): Show |
chr6 | 73456737 | 73514236 | ||
a0002c0009 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | ATGTT others(2071): Show |
chr6 | 73456737 | 73514236 | ||
a0003c0008 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | ATGTT others(2071): Show |
chr6 | 73456737 | 73514236 | ||
a0004c0005 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | ATGTT others(2071): Show |
chr6 | 73456737 | 73514236 | ||
a0005c0006 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | ATGTT others(2071): Show |
chr6 | 73456737 | 73514236 | ||
a0006c0004 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | ATGTT others(2071): Show |
chr6 | 73456737 | 73514236 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11378 | 49 | 16 | 6 | 20 | 3 | 4 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0003 | 0/0 | 11390 | 24 | 0 | 8 | 14 | 0 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11385): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0004 | 0/0 | 11385 | 21 | 0 | 6 | 15 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11380): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0005 | 0/0 | 10698 | 17 | 0 | 3 | 12 | 0 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10693): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0006 | 0/0 | 11378 | 16 | 1 | 5 | 3 | 2 | 5 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0007 | 0/0 | 11379 | 15 | 3 | 0 | 10 | 1 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0008 | 0/0 | 10697 | 10 | 7 | 0 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10692): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0009 | 0/0 | 11379 | 9 | 6 | 1 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0010 | 0/0 | 11392 | 7 | 5 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11387): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0012 | 0/0 | 11378 | 7 | 0 | 3 | 4 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0013 | 0/0 | 11378 | 7 | 0 | 5 | 0 | 2 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0014 | 0/0 | 11392 | 6 | 0 | 0 | 6 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11387): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0015 | 0/0 | 11393 | 6 | 0 | 0 | 6 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11388): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0016 | 0/0 | 11391 | 6 | 1 | 0 | 5 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0017 | 0/0 | 10698 | 4 | 4 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10693): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0018 | 0/0 | 11378 | 4 | 0 | 0 | 4 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0019 | 0/0 | 11390 | 4 | 0 | 1 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11385): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0022 | 1/0 | 10698 | 3 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10693): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0023 | 0/0 | 11381 | 3 | 0 | 1 | 0 | 2 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11376): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0024 | 0/0 | 11379 | 3 | 0 | 0 | 0 | 0 | 3 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0025 | 0/0 | 11392 | 3 | 3 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11387): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0031 | 0/0 | 10698 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10693): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0032 | 0/0 | 11386 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11381): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0033 | 0/0 | 11391 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0034 | 0/0 | 11378 | 2 | 0 | 1 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0035 | 0/0 | 11381 | 2 | 1 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11376): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0036 | 0/0 | 11378 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0037 | 0/0 | 11391 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0040 | 0/0 | 11378 | 2 | 0 | 1 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0041 | 0/0 | 10699 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10694): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0042 | 0/0 | 10697 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10692): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0043 | 0/0 | 10699 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10694): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0044 | 0/0 | 10700 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10695): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0045 | 0/0 | 10697 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10692): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0046 | 0/0 | 10697 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10692): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0047 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10690): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0048 | 0/0 | 10698 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10693): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0049 | 0/0 | 10698 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(10693): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0050 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0051 | 0/0 | 11385 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11380): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0052 | 0/0 | 11392 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11387): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0053 | 0/0 | 11392 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11387): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0054 | 0/0 | 11398 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11393): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0055 | 0/0 | 11385 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11380): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0056 | 0/0 | 11387 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11382): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0057 | 0/0 | 11393 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11388): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0058 | 0/0 | 11393 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11388): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0059 | 0/0 | 11386 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11381): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0060 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0061 | 0/0 | 11384 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11379): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0062 | 0/0 | 11392 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11387): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0065 | 0/0 | 11379 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0066 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0067 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0068 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0069 | 0/0 | 11378 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0070 | 0/0 | 11379 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0071 | 0/0 | 11395 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11390): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0072 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0073 | 0/0 | 11380 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11375): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0074 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0075 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0076 | 0/0 | 11380 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11375): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0077 | 0/0 | 11379 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0078 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0079 | 0/0 | 11378 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0080 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0081 | 0/0 | 11377 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11372): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0082 | 0/0 | 11378 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0083 | 0/0 | 11380 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11375): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0084 | 0/0 | 11379 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0085 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0086 | 0/0 | 11380 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11375): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0087 | 0/0 | 11379 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0088 | 0/0 | 11380 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11375): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0089 | 0/0 | 11379 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0090 | 0/0 | 11381 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11376): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0091 | 0/0 | 11380 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11375): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0092 | 0/0 | 11391 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0093 | 0/0 | 11378 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0094 | 0/0 | 11378 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0095 | 0/0 | 11395 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11390): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0096 | 0/0 | 11392 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11387): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0097 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0098 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0099 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0100 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0101 | 0/0 | 11392 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11387): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0102 | 0/0 | 11383 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11378): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0103 | 0/0 | 11390 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11385): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0104 | 0/0 | 11393 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11388): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0105 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0106 | 0/0 | 11390 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11385): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0107 | 0/0 | 11391 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0108 | 0/0 | 11391 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11386): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0109 | 0/0 | 11390 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11385): Show |
chr6 | 73456737 | 73514236 |
a0001c0001t0128 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0002 | 0/0 | 11396 | 29 | 0 | 4 | 21 | 2 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11391): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0011 | 0/0 | 11397 | 8 | 0 | 3 | 3 | 0 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11392): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0020 | 0/0 | 11388 | 4 | 4 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11383): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0021 | 0/0 | 11384 | 4 | 4 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11379): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0026 | 0/0 | 11395 | 2 | 0 | 1 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11390): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0027 | 0/0 | 11395 | 3 | 2 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11390): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0028 | 0/0 | 11387 | 3 | 3 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11382): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0029 | 0/0 | 11385 | 3 | 0 | 0 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11380): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0038 | 0/0 | 11395 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11390): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0039 | 0/0 | 11397 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11392): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0063 | 0/0 | 11397 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11392): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0064 | 0/0 | 11396 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11391): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0110 | 0/0 | 11396 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11391): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0111 | 0/0 | 11396 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11391): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0112 | 0/0 | 11397 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11392): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0113 | 0/0 | 11394 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11389): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0114 | 0/0 | 11396 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11391): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0115 | 0/0 | 11394 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11389): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0116 | 0/0 | 11397 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11392): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0117 | 0/0 | 11398 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11393): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0118 | 0/0 | 11397 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11392): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0119 | 0/0 | 11396 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11391): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0120 | 0/0 | 11395 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11390): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0121 | 0/0 | 11390 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11385): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0122 | 0/0 | 11390 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11385): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0123 | 0/0 | 11388 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11383): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0124 | 0/0 | 11385 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11380): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0125 | 0/0 | 11384 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11379): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0126 | 0/0 | 11386 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11381): Show |
chr6 | 73456737 | 73514236 |
a0001c0002t0127 | 0/0 | 11384 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11379): Show |
chr6 | 73456737 | 73514236 |
a0001c0003t0030 | 0/0 | 11379 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
a0001c0007t0006 | 0/1 | 11378 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0002c0009t0010 | 0/0 | 11392 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11387): Show |
chr6 | 73456737 | 73514236 |
a0003c0008t0001 | 0/0 | 11378 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11373): Show |
chr6 | 73456737 | 73514236 |
a0004c0005t0026 | 0/0 | 11395 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11390): Show |
chr6 | 73456737 | 73514236 |
a0005c0006t0004 | 0/0 | 11385 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11380): Show |
chr6 | 73456737 | 73514236 |
a0006c0004t0007 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | GTCCT others(11374): Show |
chr6 | 73456737 | 73514236 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0017g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0017g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0017g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0017g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0018g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0018g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0018g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0018g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0019g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0019g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0019g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0019g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0022g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0022g0343 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0022g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0023g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0023g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0024g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0024g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0024g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0025g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0025g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0025g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0031g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0031g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0032g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0032g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0033g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0033g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0034g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0034g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0035g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0035g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0036g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0036g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0037g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0037g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0040g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0040g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0041g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0042g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0043g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0044g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0045g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0046g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0047g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0048g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0049g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0050g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0051g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0052g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0053g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0054g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0055g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0056g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0057g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0058g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0059g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0060g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0061g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0062g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0065g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0066g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0067g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0068g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0069g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0070g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0071g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0072g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0073g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0074g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0075g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0076g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0077g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0078g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0079g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0080g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0081g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0082g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0083g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0084g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0085g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0086g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0087g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0088g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0089g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0090g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0091g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0092g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0093g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0094g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0095g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0096g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0097g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0098g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0099g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0100g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0101g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0102g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0103g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0104g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0105g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0106g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0107g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0108g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0109g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0128g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0020g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0020g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0020g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0020g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0021g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0021g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0021g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0021g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0026g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0026g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0027g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0027g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0027g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0028g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0028g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0028g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0029g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0029g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0029g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0038g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0038g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0039g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0039g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0063g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0064g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0110g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0111g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0112g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0113g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0114g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0115g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0116g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0117g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0118g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0119g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0120g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0121g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0122g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0123g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0124g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0125g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0126g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0127g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0003t0030g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0003t0030g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0007t0006g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0002c0009t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0003c0008t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0004c0005t0026g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0005c0006t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0006c0004t0007g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00099 | hp2 | a0001 | c0001 | t0023 | g0011 | EUR | GBR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00140 | hp1 | a0001 | c0001 | t0094 | g0166 | EUR | GBR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00140 | hp2 | a0001 | c0001 | t0040 | g0193 | EUR | GBR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00280 | hp1 | a0001 | c0001 | t0034 | g0149 | EUR | FIN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0148 | EUR | FIN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00323 | hp2 | a0001 | c0001 | t0082 | g0260 | EUR | FIN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00408 | hp1 | a0001 | c0001 | t0068 | g0226 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00408 | hp2 | a0001 | c0001 | t0037 | g0013 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00438 | hp1 | a0001 | c0001 | t0080 | g0175 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00438 | hp2 | a0001 | c0002 | t0039 | g0023 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00558 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00558 | hp2 | a0001 | c0001 | t0012 | g0167 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00597 | hp1 | a0001 | c0001 | t0018 | g0160 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00639 | hp1 | a0001 | c0001 | t0013 | g0180 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00642 | hp2 | a0001 | c0001 | t0023 | g0190 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00673 | hp1 | a0001 | c0001 | t0006 | g0256 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00733 | hp1 | a0001 | c0001 | t0006 | g0259 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00733 | hp2 | a0001 | c0002 | t0026 | g0005 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0282 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00735 | hp2 | a0001 | c0001 | t0109 | g0010 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0336 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00741 | hp2 | a0001 | c0001 | t0091 | g0125 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01070 | hp1 | a0001 | c0002 | t0038 | g0032 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01070 | hp2 | a0001 | c0001 | t0089 | g0248 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01074 | hp1 | a0001 | c0001 | t0013 | g0003 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01074 | hp2 | a0001 | c0001 | t0041 | g0351 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0249 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0266 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01109 | hp2 | a0001 | c0002 | t0027 | g0090 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01168 | hp1 | a0001 | c0002 | t0064 | g0319 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01168 | hp2 | a0001 | c0001 | t0071 | g0237 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0267 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01169 | hp2 | a0001 | c0002 | t0063 | g0318 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01175 | hp1 | a0001 | c0001 | t0012 | g0123 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01192 | hp1 | a0001 | c0001 | t0009 | g0310 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01192 | hp2 | a0001 | c0001 | t0013 | g0176 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0181 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0277 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01256 | hp1 | a0001 | c0001 | t0073 | g0161 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01257 | hp1 | a0001 | c0001 | t0031 | g0352 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01258 | hp1 | a0001 | c0001 | t0031 | g0348 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01261 | hp1 | a0001 | c0002 | t0011 | g0022 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01346 | hp1 | a0001 | c0001 | t0013 | g0003 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01346 | hp2 | a0001 | c0001 | t0010 | g0016 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01358 | hp2 | a0001 | c0001 | t0034 | g0138 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01433 | hp2 | a0001 | c0001 | t0040 | g0261 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0363 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01496 | hp2 | a0001 | c0002 | t0011 | g0054 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0188 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0049 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01516 | hp1 | a0001 | c0001 | t0013 | g0184 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01516 | hp2 | a0001 | c0002 | t0119 | g0070 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0252 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01517 | hp2 | a0001 | c0001 | t0013 | g0183 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01884 | hp1 | a0001 | c0002 | t0021 | g0071 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01891 | hp1 | a0001 | c0001 | t0070 | g0129 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0206 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0278 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01928 | hp2 | a0001 | c0002 | t0011 | g0031 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01934 | hp1 | a0001 | c0001 | t0106 | g0119 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0324 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0349 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01943 | hp2 | a0001 | c0001 | t0104 | g0009 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01975 | hp1 | a0001 | c0001 | t0051 | g0283 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01978 | hp1 | a0001 | c0001 | t0044 | g0357 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01978 | hp2 | a0001 | c0001 | t0012 | g0244 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01993 | hp1 | a0001 | c0001 | t0012 | g0217 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01993 | hp2 | a0001 | c0002 | t0038 | g0030 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02004 | hp1 | a0001 | c0001 | t0052 | g0279 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02004 | hp2 | a0001 | c0001 | t0019 | g0116 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02015 | hp1 | a0001 | c0001 | t0075 | g0231 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0315 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02027 | hp1 | a0001 | c0001 | t0128 | g0139 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02040 | hp2 | a0001 | c0001 | t0008 | g0122 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02055 | hp1 | a0001 | c0001 | t0048 | g0340 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02055 | hp2 | a0001 | c0001 | t0088 | g0189 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0233 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02074 | hp1 | a0001 | c0001 | t0018 | g0159 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02080 | hp2 | a0001 | c0002 | t0039 | g0040 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02129 | hp2 | a0001 | c0001 | t0008 | g0120 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02132 | hp1 | a0001 | c0002 | t0116 | g0063 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02132 | hp2 | a0001 | c0001 | t0015 | g0014 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02135 | hp2 | a0001 | c0001 | t0078 | g0156 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0191 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02145 | hp2 | a0001 | c0001 | t0093 | g0192 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02155 | hp1 | a0001 | c0002 | t0110 | g0046 | EAS | CDX | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | CDX | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02165 | hp1 | a0001 | c0002 | t0124 | g0007 | EAS | CDX | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02165 | hp2 | a0001 | c0001 | t0012 | g0224 | EAS | CDX | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02257 | hp1 | a0001 | c0002 | t0020 | g0072 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0341 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02273 | hp1 | a0001 | c0001 | t0107 | g0107 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02273 | hp2 | a0001 | c0001 | t0103 | g0008 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02280 | hp2 | a0002 | c0009 | t0010 | g0276 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0200 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02300 | hp2 | a0001 | c0001 | t0102 | g0108 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02451 | hp1 | a0001 | c0002 | t0113 | g0005 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02451 | hp2 | a0001 | c0001 | t0069 | g0250 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02572 | hp2 | a0001 | c0002 | t0125 | g0086 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02615 | hp1 | a0001 | c0002 | t0122 | g0085 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0305 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02622 | hp2 | a0001 | c0001 | t0025 | g0141 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02630 | hp2 | a0001 | c0001 | t0022 | g0333 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02647 | hp1 | a0001 | c0003 | t0030 | g0355 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02647 | hp2 | a0001 | c0001 | t0047 | g0019 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02717 | hp1 | a0001 | c0002 | t0028 | g0074 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02717 | hp2 | a0001 | c0001 | t0099 | g0137 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02738 | hp2 | a0001 | c0002 | t0011 | g0068 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02809 | hp2 | a0001 | c0001 | t0010 | g0299 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02818 | hp1 | a0001 | c0002 | t0027 | g0092 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02818 | hp2 | a0001 | c0002 | t0121 | g0081 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0197 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02896 | hp1 | a0001 | c0002 | t0020 | g0076 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02896 | hp2 | a0001 | c0001 | t0035 | g0135 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02897 | hp2 | a0001 | c0001 | t0062 | g0017 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02922 | hp2 | a0001 | c0001 | t0025 | g0140 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0339 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02965 | hp2 | a0001 | c0002 | t0021 | g0080 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02970 | hp2 | a0001 | c0001 | t0017 | g0337 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0251 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0360 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0347 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03041 | hp2 | a0001 | c0002 | t0021 | g0087 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03098 | hp1 | a0001 | c0001 | t0098 | g0320 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0302 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03130 | hp2 | a0001 | c0002 | t0020 | g0078 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03195 | hp1 | a0001 | c0001 | t0076 | g0271 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03209 | hp1 | a0001 | c0001 | t0025 | g0142 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0185 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0338 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03239 | hp1 | a0001 | c0002 | t0011 | g0006 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03239 | hp2 | a0001 | c0001 | t0024 | g0258 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03453 | hp1 | a0001 | c0001 | t0022 | g0344 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03453 | hp2 | a0001 | c0001 | t0090 | g0124 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03491 | hp1 | a0001 | c0001 | t0043 | g0346 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0055 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03516 | hp1 | a0001 | c0001 | t0017 | g0362 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0316 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03540 | hp2 | a0001 | c0002 | t0028 | g0077 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0332 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0359 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0219 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03669 | hp2 | a0001 | c0001 | t0024 | g0264 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03688 | hp1 | a0001 | c0001 | t0024 | g0257 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03688 | hp2 | a0001 | c0001 | t0079 | g0162 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03710 | hp1 | a0003 | c0008 | t0001 | g0223 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03710 | hp2 | a0001 | c0001 | t0087 | g0229 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03927 | hp1 | a0001 | c0001 | t0077 | g0169 | SAS | BEB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03927 | hp2 | a0001 | c0001 | t0054 | g0247 | SAS | BEB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0037 | SAS | BEB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0262 | SAS | BEB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04115 | hp1 | a0001 | c0001 | t0092 | g0222 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0265 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0194 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0187 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18522 | hp1 | a0001 | c0001 | t0017 | g0358 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0303 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | CHB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18612 | hp2 | a0001 | c0001 | t0015 | g0013 | EAS | CHB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0127 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18906 | hp2 | a0001 | c0001 | t0017 | g0361 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18943 | hp2 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18944 | hp1 | a0001 | c0001 | t0014 | g0205 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18944 | hp2 | a0001 | c0001 | t0018 | g0147 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18945 | hp2 | a0001 | c0001 | t0012 | g0220 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18946 | hp2 | a0001 | c0001 | t0016 | g0094 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18948 | hp1 | a0001 | c0001 | t0014 | g0314 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18948 | hp2 | a0001 | c0002 | t0026 | g0043 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18951 | hp2 | a0001 | c0002 | t0118 | g0369 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18957 | hp1 | a0001 | c0001 | t0016 | g0367 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18957 | hp2 | a0001 | c0001 | t0037 | g0285 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18962 | hp1 | a0001 | c0001 | t0035 | g0177 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18962 | hp2 | a0001 | c0001 | t0057 | g0295 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18965 | hp1 | a0001 | c0001 | t0016 | g0186 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18965 | hp2 | a0001 | c0001 | t0059 | g0322 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0350 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18969 | hp1 | a0001 | c0001 | t0074 | g0221 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18969 | hp2 | a0001 | c0002 | t0029 | g0007 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18971 | hp1 | a0001 | c0001 | t0012 | g0168 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18971 | hp2 | a0001 | c0001 | t0007 | g0179 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18972 | hp1 | a0001 | c0001 | t0008 | g0121 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18972 | hp2 | a0001 | c0001 | t0016 | g0093 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18973 | hp2 | a0001 | c0001 | t0014 | g0298 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18975 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18975 | hp2 | a0001 | c0001 | t0101 | g0095 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18978 | hp1 | a0001 | c0001 | t0085 | g0171 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18978 | hp2 | a0004 | c0005 | t0026 | g0028 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18979 | hp1 | a0001 | c0001 | t0032 | g0297 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18980 | hp2 | a0001 | c0001 | t0055 | g0291 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18981 | hp1 | a0001 | c0002 | t0011 | g0061 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18982 | hp2 | a0001 | c0001 | t0081 | g0253 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18984 | hp2 | a0001 | c0001 | t0067 | g0157 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18987 | hp1 | a0001 | c0001 | t0007 | g0212 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18987 | hp2 | a0001 | c0002 | t0011 | g0029 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18989 | hp2 | a0001 | c0001 | t0049 | g0342 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18990 | hp2 | a0005 | c0006 | t0004 | g0296 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0365 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18991 | hp2 | a0001 | c0001 | t0015 | g0328 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18995 | hp1 | a0001 | c0001 | t0015 | g0287 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18995 | hp2 | a0001 | c0001 | t0015 | g0294 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18999 | hp1 | a0001 | c0001 | t0032 | g0323 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19000 | hp1 | a0001 | c0002 | t0127 | g0082 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19000 | hp2 | a0001 | c0002 | t0117 | g0067 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19001 | hp2 | a0001 | c0001 | t0058 | g0289 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19002 | hp1 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19002 | hp2 | a0001 | c0001 | t0086 | g0150 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19003 | hp2 | a0001 | c0001 | t0015 | g0286 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19007 | hp2 | a0001 | c0001 | t0014 | g0211 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19009 | hp1 | a0001 | c0001 | t0036 | g0164 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19009 | hp2 | a0001 | c0001 | t0033 | g0097 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19010 | hp2 | a0001 | c0001 | t0019 | g0101 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19011 | hp1 | a0001 | c0002 | t0112 | g0366 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19012 | hp1 | a0001 | c0001 | t0096 | g0202 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19012 | hp2 | a0001 | c0001 | t0036 | g0174 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19030 | hp1 | a0001 | c0002 | t0020 | g0075 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19030 | hp2 | a0001 | c0002 | t0126 | g0088 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19043 | hp1 | a0001 | c0002 | t0021 | g0089 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0313 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19055 | hp2 | a0001 | c0001 | t0014 | g0288 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19056 | hp1 | a0006 | c0004 | t0007 | g0312 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0353 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19058 | hp1 | a0001 | c0001 | t0066 | g0154 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19058 | hp2 | a0001 | c0001 | t0061 | g0301 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19062 | hp1 | a0001 | c0001 | t0014 | g0329 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19063 | hp1 | a0001 | c0001 | t0019 | g0105 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0356 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19064 | hp1 | a0001 | c0002 | t0029 | g0083 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19066 | hp1 | a0001 | c0002 | t0111 | g0062 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19066 | hp2 | a0001 | c0001 | t0007 | g0145 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19067 | hp1 | a0001 | c0001 | t0019 | g0100 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19067 | hp2 | a0001 | c0001 | t0009 | g0238 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0335 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19077 | hp1 | a0001 | c0001 | t0095 | g0284 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19077 | hp2 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19081 | hp1 | a0001 | c0001 | t0018 | g0144 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19082 | hp1 | a0001 | c0001 | t0056 | g0321 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19082 | hp2 | a0001 | c0001 | t0007 | g0326 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19083 | hp1 | a0001 | c0001 | t0060 | g0173 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19083 | hp2 | a0001 | c0002 | t0115 | g0024 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0255 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19085 | hp2 | a0001 | c0002 | t0029 | g0084 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19086 | hp1 | a0001 | c0002 | t0114 | g0033 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19086 | hp2 | a0001 | c0001 | t0007 | g0304 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19087 | hp1 | a0001 | c0001 | t0007 | g0146 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19087 | hp2 | a0001 | c0002 | t0011 | g0059 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19088 | hp1 | a0001 | c0001 | t0072 | g0228 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19090 | hp1 | a0001 | c0001 | t0050 | g0151 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19090 | hp2 | a0001 | c0001 | t0108 | g0096 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19091 | hp1 | a0001 | c0001 | t0016 | g0368 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19091 | hp2 | a0001 | c0001 | t0007 | g0232 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19240 | hp1 | a0001 | c0002 | t0123 | g0073 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19240 | hp2 | a0001 | c0001 | t0046 | g0330 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20129 | hp1 | a0001 | c0002 | t0028 | g0079 | AFR | ASW | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20752 | hp1 | a0001 | c0001 | t0023 | g0011 | EUR | TSI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20752 | hp2 | a0001 | c0001 | t0065 | g0152 | EUR | TSI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0034 | EUR | TSI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | TSI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20905 | hp1 | a0001 | c0001 | t0083 | g0263 | SAS | GIH | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20905 | hp2 | a0001 | c0001 | t0084 | g0216 | SAS | GIH | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01123 | hp1 | a0001 | c0001 | t0010 | g0016 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0198 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0126 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02486 | hp2 | a0001 | c0001 | t0053 | g0209 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03471 | hp1 | a0001 | c0002 | t0027 | g0091 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03471 | hp2 | a0001 | c0001 | t0100 | g0153 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG06807 | hp1 | a0001 | c0003 | t0030 | g0354 | AFR | USA | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG06807 | hp2 | a0001 | c0001 | t0045 | g0345 | AFR | USA | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18955 | hp1 | a0001 | c0002 | t0120 | g0065 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18955 | hp2 | a0001 | c0001 | t0042 | g0364 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20300 | hp1 | a0001 | c0001 | t0105 | g0103 | AFR | USA | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20300 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | USA | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA21309 | hp1 | a0001 | c0001 | t0097 | g0143 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
homoSapiens | chm13v2 | a0001 | c0007 | t0006 | g0254 | REF | REF | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
homoSapiens | grch38p0 | a0001 | c0001 | t0022 | g0343 | REF | REF | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:73461903 | A | G | 1 | a0002 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.49A>G | p.Lys17Glu | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/12 | 167/10698 | 49/2079 | 17/692 | chr6 | 73461903 | |||
chr6:73461925 | G | C | 1 | a0006 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.71G>C | p.Arg24Pro | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/12 | 189/10698 | 71/2079 | 24/692 | chr6 | 73461925 | |||
chr6:73466298 | A | G | 1 | a0003 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.307A>G | p.Ile103Val | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 2/12 | 425/10698 | 307/2079 | 103/692 | chr6 | 73466298 | |||
chr6:73482620 | G | C | 1 | a0005 | 1 | NA18990.hp2 | missense_variant&splice_region_variant | MODERATE | c.1637G>C | p.Arg546Thr | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/12 | 1755/10698 | 1637/2079 | 546/692 | chr6 | 73482620 | |||
chr6:73492263 | T | C | 1 | a0004 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.1667T>C | p.Val556Ala | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/12 | 1785/10698 | 1667/2079 | 556/692 | chr6 | 73492263 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:73480725 | T | C | 2 | a0001c0002 a0004c0005 |
81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
synonymous_variant | LOW | c.1180T>C | p.Leu394Leu | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/12 | 1298/10698 | 1180/2079 | 394/692 | chr6 | 73480725 | |||
chr6:73482147 | T | C | 1 | a0001c0003 | 2 | HG02647.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.1368T>C | p.Thr456Thr | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 8/12 | 1486/10698 | 1368/2079 | 456/692 | chr6 | 73482147 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:73461744 | C | G | 118 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(115): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
5_prime_UTR_variant | MODIFIER | c.-111C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/12 | 111 | chr6 | 73461744 | ||||||
chr6:73461795 | G | C | 1 | a0001c0001t0050 | 1 | NA19090.hp1 | 5_prime_UTR_variant | MODIFIER | c.-60G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/12 | 60 | chr6 | 73461795 | ||||||
chr6:73500864 | C | G | 1 | a0001c0001t0128 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*129C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 129 | chr6 | 73500864 | ||||||
chr6:73500897 | C | T | 11 | a0001c0002t0020 a0001c0002t0021 a0001c0002t0028 others(8): Show |
21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*162C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 162 | chr6 | 73500897 | ||||||
chr6:73501230 | G | T | 1 | a0001c0001t0049 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 495 | chr6 | 73501230 | ||||||
chr6:73501545 | C | G | 1 | a0001c0001t0040 | 2 | HG00140.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*810C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 810 | chr6 | 73501545 | ||||||
chr6:73501997 | A | T | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1262A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1262 | chr6 | 73501997 | ||||||
chr6:73502358 | C | T | 17 | a0001c0002t0002 a0001c0002t0011 a0001c0002t0026 others(14): Show |
55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1623C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1623 | chr6 | 73502358 | ||||||
chr6:73502451 | AAAAAG | A | 6 | a0001c0002t0021 a0001c0002t0029 a0001c0002t0124 others(3): Show |
11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1724_*1728delAAGA others(1): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1724 | INFO_REALIGN_3_PRIME | chr6 | 73502451 | |||||
chr6:73502601 | TAAAG | T | 11 | a0001c0002t0020 a0001c0002t0021 a0001c0002t0028 others(8): Show |
21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1870_*1873delGAAA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1870 | INFO_REALIGN_3_PRIME | chr6 | 73502601 | |||||
chr6:73502620 | C | T | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1885C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1885 | chr6 | 73502620 | ||||||
chr6:73502895 | C | CA | 23 | a0001c0001t0033 a0001c0001t0041 a0001c0001t0060 others(20): Show |
62 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2173dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2174 | INFO_REALIGN_3_PRIME | chr6 | 73502895 | |||||
chr6:73502895 | C | CAA | 16 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0014 others(13): Show |
53 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2172_*2173dupAA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2174 | INFO_REALIGN_3_PRIME | chr6 | 73502895 | |||||
chr6:73502956 | T | C | 1 | a0001c0002t0110 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2221T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2221 | chr6 | 73502956 | ||||||
chr6:73502996 | G | A | 2 | a0001c0001t0034 a0001c0001t0065 |
3 | HG00280.hp1 HG01358.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2261G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2261 | chr6 | 73502996 | ||||||
chr6:73503104 | G | A | 49 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(46): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*2369G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2369 | chr6 | 73503104 | ||||||
chr6:73503112 | C | T | 60 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(57): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*2377C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2377 | chr6 | 73503112 | ||||||
chr6:73503172 | A | G | 1 | a0001c0001t0094 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2437A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2437 | chr6 | 73503172 | ||||||
chr6:73503288 | T | A | 2 | a0001c0001t0066 a0001c0001t0067 |
2 | NA18984.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2553T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2553 | chr6 | 73503288 | ||||||
chr6:73503314 | T | C | 1 | a0001c0001t0012 | 7 | HG00558.hp2 HG01175.hp1 HG01978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2579T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2579 | chr6 | 73503314 | ||||||
chr6:73503524 | T | C | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2789T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2789 | chr6 | 73503524 | ||||||
chr6:73503670 | T | C | 21 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0014 others(18): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2935T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2935 | chr6 | 73503670 | ||||||
chr6:73503774 | G | C | 1 | a0001c0001t0013 | 7 | HG00639.hp1 HG01074.hp1 HG01192.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3039G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3039 | chr6 | 73503774 | ||||||
chr6:73503795 | T | G | 1 | a0001c0001t0068 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3060T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3060 | chr6 | 73503795 | ||||||
chr6:73503884 | T | C | 1 | a0001c0002t0121 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3149T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3149 | chr6 | 73503884 | ||||||
chr6:73504232 | A | G | 1 | a0001c0001t0036 | 2 | NA19009.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3497A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3497 | chr6 | 73504232 | ||||||
chr6:73504261 | A | C | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3526A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3526 | chr6 | 73504261 | ||||||
chr6:73504283 | C | T | 11 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0033 others(8): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3548C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3548 | chr6 | 73504283 | ||||||
chr6:73504350 | C | T | 1 | a0001c0001t0093 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3615C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3615 | chr6 | 73504350 | ||||||
chr6:73504418 | A | G | 1 | a0001c0001t0018 | 4 | HG00597.hp1 HG02074.hp1 NA18944.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3683A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3683 | chr6 | 73504418 | ||||||
chr6:73504707 | C | G | 1 | a0001c0001t0059 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3972C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3972 | chr6 | 73504707 | ||||||
chr6:73504715 | C | T | 11 | a0001c0002t0020 a0001c0002t0021 a0001c0002t0027 others(8): Show |
23 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3980C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3980 | chr6 | 73504715 | ||||||
chr6:73504828 | G | A | 1 | a0001c0001t0069 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4093G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4093 | chr6 | 73504828 | ||||||
chr6:73504953 | G | A | 1 | a0001c0001t0070 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4218G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4218 | chr6 | 73504953 | ||||||
chr6:73505181 | C | CA | 20 | a0001c0001t0071 a0001c0002t0002 a0001c0002t0011 others(17): Show |
60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4458dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4459 | INFO_REALIGN_3_PRIME | chr6 | 73505181 | |||||
chr6:73505194 | T | A | 3 | a0001c0001t0025 a0001c0001t0097 a0001c0001t0098 |
5 | HG02622.hp2 HG02922.hp2 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4459T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4459 | chr6 | 73505194 | ||||||
chr6:73505256 | G | A | 1 | a0001c0001t0051 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4521G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4521 | chr6 | 73505256 | ||||||
chr6:73505320 | G | A | 11 | a0001c0002t0020 a0001c0002t0021 a0001c0002t0028 others(8): Show |
21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4585G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4585 | chr6 | 73505320 | ||||||
chr6:73505394 | C | T | 1 | a0001c0001t0040 | 2 | HG00140.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4659C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4659 | chr6 | 73505394 | ||||||
chr6:73505403 | A | C | 1 | a0001c0001t0040 | 2 | HG00140.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4668A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4668 | chr6 | 73505403 | ||||||
chr6:73505537 | AT | A | 19 | a0001c0001t0071 a0001c0002t0002 a0001c0002t0011 others(16): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4805delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4805 | INFO_REALIGN_3_PRIME | chr6 | 73505537 | |||||
chr6:73505551 | GTTTTGTT others(5): Show |
G | 47 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(44): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*4828_*4839delTTTT others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4828 | INFO_REALIGN_3_PRIME | chr6 | 73505551 | |||||
chr6:73505562 | G | A | 4 | a0001c0001t0015 a0001c0001t0037 a0001c0001t0095 others(1): Show |
10 | HG00408.hp2 HG02132.hp2 NA18612.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4827G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4827 | chr6 | 73505562 | ||||||
chr6:73505691 | T | C | 2 | a0001c0002t0111 a0001c0002t0112 |
2 | NA19011.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4956T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4956 | chr6 | 73505691 | ||||||
chr6:73505745 | G | A | 7 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0041 others(4): Show |
24 | HG00741.hp1 HG01074.hp2 HG01257.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5010G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5010 | chr6 | 73505745 | ||||||
chr6:73506134 | A | G | 1 | a0001c0001t0109 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5399A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5399 | chr6 | 73506134 | ||||||
chr6:73506293 | T | C | 1 | a0001c0001t0097 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5558T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5558 | chr6 | 73506293 | ||||||
chr6:73506478 | G | A | 61 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(58): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*5743G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5743 | chr6 | 73506478 | ||||||
chr6:73506551 | A | G | 17 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0014 others(14): Show |
55 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*5816A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5816 | chr6 | 73506551 | ||||||
chr6:73506682 | C | CT | 27 | a0001c0001t0043 a0001c0001t0048 a0001c0001t0054 others(24): Show |
69 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*5970dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5971 | INFO_REALIGN_3_PRIME | chr6 | 73506682 | |||||
chr6:73506682 | C | CTT | 9 | a0001c0001t0044 a0001c0002t0029 a0001c0002t0039 others(6): Show |
12 | HG00438.hp2 HG01978.hp1 HG02080.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5969_*5970dupTT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5971 | INFO_REALIGN_3_PRIME | chr6 | 73506682 | |||||
chr6:73506682 | CT | C | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(55): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*5970delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5970 | INFO_REALIGN_3_PRIME | chr6 | 73506682 | |||||
chr6:73506682 | CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0004 a0001c0001t0032 a0001c0001t0051 others(6): Show |
30 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5963_*5970delTTTT others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5963 | INFO_REALIGN_3_PRIME | chr6 | 73506682 | |||||
chr6:73506749 | C | T | 9 | a0001c0001t0006 a0001c0001t0023 a0001c0001t0024 others(6): Show |
29 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*6014C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6014 | chr6 | 73506749 | ||||||
chr6:73506879 | G | C | 6 | a0001c0002t0021 a0001c0002t0029 a0001c0002t0124 others(3): Show |
11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6144G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6144 | chr6 | 73506879 | ||||||
chr6:73506914 | C | CCTGACCT others(689): Show |
3 | a0001c0001t0025 a0001c0001t0097 a0001c0001t0099 |
5 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(688): Show |
1 | a0001c0001t0081 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(691): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(690): Show |
1 | a0001c0001t0072 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(693): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(689): Show |
45 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(42): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(689): Show |
9 | a0001c0001t0103 a0001c0002t0021 a0001c0002t0029 others(6): Show |
14 | HG01884.hp1 HG02165.hp1 HG02273.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(689): Show |
30 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(27): Show |
95 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(689): Show |
3 | a0001c0002t0020 a0001c0002t0028 a0001c0002t0123 |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(690): Show |
4 | a0001c0001t0015 a0001c0001t0037 a0001c0001t0056 others(1): Show |
10 | HG00408.hp2 HG02132.hp2 NA18612.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(693): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(690): Show |
21 | a0001c0001t0054 a0001c0001t0071 a0001c0001t0095 others(18): Show |
59 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(693): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(691): Show |
1 | a0001c0002t0116 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(694): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506914 | C | CCTGACCT others(690): Show |
1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(693): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | |||||
chr6:73506996 | C | T | 1 | a0001c0001t0106 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6261C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6261 | chr6 | 73506996 | ||||||
chr6:73507070 | A | G | 6 | a0001c0002t0021 a0001c0002t0029 a0001c0002t0124 others(3): Show |
11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6335A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6335 | chr6 | 73507070 | ||||||
chr6:73507220 | T | G | 47 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(44): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*6485T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6485 | chr6 | 73507220 | ||||||
chr6:73507385 | A | G | 1 | a0001c0002t0118 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6650A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6650 | chr6 | 73507385 | ||||||
chr6:73507547 | G | A | 15 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0015 others(12): Show |
48 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*6812G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6812 | chr6 | 73507547 | ||||||
chr6:73507555 | G | A | 119 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(116): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
3_prime_UTR_variant | MODIFIER | c.*6820G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6820 | chr6 | 73507555 | ||||||
chr6:73507703 | T | C | 1 | a0001c0002t0121 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6968T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6968 | chr6 | 73507703 | ||||||
chr6:73507705 | C | T | 1 | a0001c0001t0128 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6970C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6970 | chr6 | 73507705 | ||||||
chr6:73507715 | C | A | 28 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0058 others(25): Show |
71 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*6980C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6980 | chr6 | 73507715 | ||||||
chr6:73507793 | T | A | 1 | a0001c0001t0055 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7058T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7058 | chr6 | 73507793 | ||||||
chr6:73507793 | T | C | 1 | a0001c0001t0084 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7058T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7058 | chr6 | 73507793 | ||||||
chr6:73507801 | C | A | 2 | a0001c0001t0046 a0001c0001t0074 |
2 | NA18969.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7066C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7066 | chr6 | 73507801 | ||||||
chr6:73507807 | G | C | 3 | a0001c0001t0055 a0001c0001t0068 a0001c0001t0075 |
3 | HG00408.hp1 HG02015.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7072G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7072 | chr6 | 73507807 | ||||||
chr6:73507837 | T | C | 132 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(129): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
3_prime_UTR_variant | MODIFIER | c.*7102T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7102 | chr6 | 73507837 | ||||||
chr6:73507843 | G | A | 2 | a0001c0001t0098 a0001c0001t0100 |
2 | HG03098.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7108G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7108 | chr6 | 73507843 | ||||||
chr6:73507845 | T | C | 5 | a0001c0001t0031 a0001c0001t0071 a0001c0001t0098 others(2): Show |
6 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7110T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7110 | chr6 | 73507845 | ||||||
chr6:73507847 | C | G | 132 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(129): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
3_prime_UTR_variant | MODIFIER | c.*7112C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7112 | chr6 | 73507847 | ||||||
chr6:73507869 | C | T | 1 | a0001c0001t0068 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7134C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7134 | chr6 | 73507869 | ||||||
chr6:73507894 | G | A | 1 | a0001c0001t0085 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7159G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7159 | chr6 | 73507894 | ||||||
chr6:73507932 | G | A | 3 | a0001c0001t0019 a0001c0001t0053 a0001c0001t0107 |
6 | HG02004.hp2 HG02273.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7197G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7197 | chr6 | 73507932 | ||||||
chr6:73507933 | C | T | 3 | a0001c0001t0019 a0001c0001t0053 a0001c0001t0107 |
6 | HG02004.hp2 HG02273.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7198C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7198 | chr6 | 73507933 | ||||||
chr6:73507946 | T | C | 1 | a0001c0001t0082 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7211T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7211 | chr6 | 73507946 | ||||||
chr6:73507956 | G | T | 1 | a0001c0002t0127 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7221G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7221 | chr6 | 73507956 | ||||||
chr6:73507976 | CA | C | 28 | a0001c0001t0008 a0001c0001t0025 a0001c0001t0045 others(25): Show |
72 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*7265delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7265 | INFO_REALIGN_3_PRIME | chr6 | 73507976 | |||||
chr6:73507976 | CAA | C | 23 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0024 others(20): Show |
50 | HG00280.hp2 HG01516.hp2 HG01884.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*7264_*7265delAA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7264 | INFO_REALIGN_3_PRIME | chr6 | 73507976 | |||||
chr6:73507976 | CAAA | C | 66 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(63): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*7263_*7265delAAA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7263 | INFO_REALIGN_3_PRIME | chr6 | 73507976 | |||||
chr6:73508101 | T | A | 1 | a0001c0002t0123 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7366T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7366 | chr6 | 73508101 | ||||||
chr6:73508210 | T | C | 1 | a0001c0001t0043 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7475T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7475 | chr6 | 73508210 | ||||||
chr6:73508311 | T | C | 1 | a0001c0001t0079 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7576T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7576 | chr6 | 73508311 | ||||||
chr6:73508418 | T | C | 2 | a0001c0001t0077 a0001c0001t0087 |
2 | HG03710.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7683T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7683 | chr6 | 73508418 | ||||||
chr6:73508482 | A | T | 1 | a0001c0001t0076 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7747A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7747 | chr6 | 73508482 | ||||||
chr6:73508557 | A | C | 10 | a0001c0001t0016 a0001c0001t0025 a0001c0001t0047 others(7): Show |
22 | HG02257.hp1 HG02622.hp2 HG02647.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*7822A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7822 | chr6 | 73508557 | ||||||
chr6:73508573 | A | G | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7838A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7838 | chr6 | 73508573 | ||||||
chr6:73508671 | G | C | 2 | a0001c0001t0078 a0001c0001t0080 |
2 | HG00438.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7936G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7936 | chr6 | 73508671 | ||||||
chr6:73509040 | A | T | 4 | a0001c0001t0047 a0001c0002t0020 a0001c0002t0028 others(1): Show |
9 | HG02257.hp1 HG02647.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8305A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 8305 | chr6 | 73509040 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:73462271 | A | G | 1 | a0001c0002t0118g0369 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.217+200A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462271 | |||||||
chr6:73462331 | C | T | 3 | a0001c0001t0016g0367 a0001c0001t0016g0368 a0001c0002t0112g0366 |
3 | NA18957.hp1 NA19011.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.217+260C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462331 | |||||||
chr6:73462344 | G | GAGA | 79 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(76): Show |
79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+273_217+274ins others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462344 | |||||||
chr6:73462347 | A | T | 79 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(76): Show |
79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+276A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462347 | |||||||
chr6:73462349 | C | A | 79 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(76): Show |
79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+278C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462349 | |||||||
chr6:73462350 | A | AG | 79 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(76): Show |
79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+279_217+280ins others(1): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462350 | |||||||
chr6:73462352 | C | A | 79 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(76): Show |
79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+281C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462352 | |||||||
chr6:73462624 | G | C | 5 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0367 others(2): Show |
5 | NA18946.hp2 NA18957.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+553G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462624 | |||||||
chr6:73462654 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.217+583G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462654 | |||||||
chr6:73462664 | G | A | 55 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(52): Show |
55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.217+593G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462664 | |||||||
chr6:73462684 | C | G | 1 | a0001c0002t0119g0070 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.217+613C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462684 | |||||||
chr6:73462753 | A | T | 7 | a0001c0002t0021g0087 a0001c0002t0021g0089 a0001c0002t0027g0090 others(4): Show |
7 | HG01109.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+682A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462753 | |||||||
chr6:73462798 | A | G | 1 | a0001c0002t0002g0069 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.217+727A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462798 | |||||||
chr6:73462863 | G | A | 55 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(52): Show |
55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.217+792G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462863 | |||||||
chr6:73462867 | G | A | 3 | a0001c0001t0008g0120 a0001c0001t0008g0121 a0001c0001t0008g0122 |
3 | HG02040.hp2 HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.217+796G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462867 | |||||||
chr6:73463000 | T | C | 336 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(333): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.217+929T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463000 | |||||||
chr6:73463008 | G | A | 1 | a0001c0001t0012g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.217+937G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463008 | |||||||
chr6:73463020 | C | CT | 9 | a0001c0001t0001g0327 a0001c0001t0005g0365 a0001c0001t0007g0326 others(6): Show |
9 | HG02615.hp1 HG02738.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.217+965dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73463020 | ||||||
chr6:73463020 | CTTT | C | 32 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(29): Show |
37 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+963_217+965del others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73463020 | ||||||
chr6:73463273 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.217+1202C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463273 | |||||||
chr6:73463292 | A | G | 2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.217+1221A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463292 | |||||||
chr6:73463333 | A | G | 1 | a0001c0001t0006g0324 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.217+1262A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463333 | |||||||
chr6:73463709 | T | C | 5 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0009g0128 others(2): Show |
5 | HG00741.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+1638T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463709 | |||||||
chr6:73463833 | C | T | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.217+1762C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463833 | |||||||
chr6:73463951 | G | A | 1 | a0001c0001t0046g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.217+1880G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463951 | |||||||
chr6:73464296 | C | G | 3 | a0001c0001t0008g0120 a0001c0001t0008g0121 a0001c0001t0008g0122 |
3 | HG02040.hp2 HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.218-1913C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464296 | |||||||
chr6:73464402 | C | T | 3 | a0001c0001t0032g0323 a0001c0001t0056g0321 a0001c0001t0059g0322 |
3 | NA18965.hp2 NA18999.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.218-1807C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464402 | |||||||
chr6:73464441 | A | G | 1 | a0001c0001t0098g0320 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218-1768A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464441 | |||||||
chr6:73464638 | C | T | 77 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(74): Show |
77 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.218-1571C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464638 | |||||||
chr6:73464659 | T | TA | 13 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0133 others(10): Show |
16 | HG01891.hp1 HG02056.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.218-1533dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464659 | ||||||
chr6:73464659 | TA | T | 29 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(26): Show |
29 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-1533delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464659 | ||||||
chr6:73464671 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.218-1538A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464671 | |||||||
chr6:73464673 | A | G | 2 | a0001c0001t0001g0317 a0001c0001t0007g0316 |
2 | HG01109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.218-1536A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464673 | |||||||
chr6:73464790 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.218-1419G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464790 | |||||||
chr6:73464801 | C | T | 4 | a0001c0002t0021g0087 a0001c0002t0021g0089 a0001c0002t0125g0086 others(1): Show |
4 | HG02572.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-1408C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464801 | |||||||
chr6:73464803 | C | A | 1 | a0001c0001t0003g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.218-1406C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464803 | |||||||
chr6:73464826 | ACT | A | 12 | a0001c0002t0021g0080 a0001c0002t0021g0087 a0001c0002t0021g0089 others(9): Show |
12 | HG02165.hp1 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.218-1380_218-1379d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464826 | ||||||
chr6:73464835 | C | CA | 90 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0165 others(87): Show |
92 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.218-1348dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464835 | ||||||
chr6:73464835 | C | CAA | 13 | a0001c0001t0001g0136 a0001c0001t0007g0145 a0001c0001t0007g0146 others(10): Show |
13 | HG00280.hp1 HG00280.hp2 HG03471.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-1349_218-1348d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464835 | ||||||
chr6:73464835 | C | CAAA | 8 | a0001c0001t0025g0140 a0001c0001t0025g0141 a0001c0001t0025g0142 others(5): Show |
8 | HG01358.hp2 HG02027.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-1350_218-1348d others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464835 | ||||||
chr6:73464835 | CA | C | 8 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0005g0365 others(5): Show |
8 | HG01884.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-1348delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464835 | ||||||
chr6:73464846 | A | C | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.218-1363A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464846 | |||||||
chr6:73464859 | A | AAC | 9 | a0001c0002t0020g0072 a0001c0002t0021g0080 a0001c0002t0028g0074 others(6): Show |
9 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.218-1349_218-1348i others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464859 | ||||||
chr6:73464859 | A | AC | 18 | a0001c0002t0002g0025 a0001c0002t0002g0026 a0001c0002t0002g0027 others(15): Show |
18 | HG00438.hp2 HG01261.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-1350_218-1349i others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464859 | |||||||
chr6:73464859 | A | C | 53 | a0001c0002t0002g0006 a0001c0002t0002g0034 a0001c0002t0002g0035 others(50): Show |
53 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.218-1350A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464859 | |||||||
chr6:73464994 | A | G | 2 | a0001c0001t0005g0365 a0001c0001t0042g0364 |
2 | NA18955.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.218-1215A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464994 | |||||||
chr6:73465218 | C | T | 1 | a0001c0001t0014g0211 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.218-991C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465218 | |||||||
chr6:73465276 | G | A | 1 | a0001c0001t0099g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.218-933G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465276 | |||||||
chr6:73465403 | A | G | 1 | a0001c0001t0003g0114 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.218-806A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465403 | |||||||
chr6:73465443 | C | T | 8 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-766C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465443 | |||||||
chr6:73465459 | C | T | 20 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(17): Show |
20 | HG02165.hp1 HG02257.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.218-750C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465459 | |||||||
chr6:73465469 | T | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0158 others(89): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.218-740T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465469 | |||||||
chr6:73465611 | T | A | 1 | a0001c0002t0002g0064 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.218-598T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465611 | |||||||
chr6:73465715 | G | A | 1 | a0001c0002t0011g0029 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.218-494G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465715 | |||||||
chr6:73465869 | G | A | 336 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(333): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.218-340G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465869 | |||||||
chr6:73465899 | G | A | 1 | a0001c0001t0054g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.218-310G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465899 | |||||||
chr6:73466171 | G | A | 14 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(11): Show |
14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.218-38G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73466171 | |||||||
chr6:73466658 | G | A | 5 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.535+52G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73466658 | |||||||
chr6:73466946 | TTATA | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.535+346_535+349del others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73466946 | ||||||
chr6:73466997 | TC | T | 8 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+392delC | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73466997 | |||||||
chr6:73467124 | G | A | 5 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.535+518G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467124 | |||||||
chr6:73467144 | T | C | 3 | a0001c0001t0025g0140 a0001c0001t0025g0141 a0001c0001t0025g0142 |
3 | HG02622.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.535+538T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467144 | |||||||
chr6:73467263 | G | A | 57 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.535+657G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467263 | |||||||
chr6:73467614 | A | AAAAT | 95 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(92): Show |
102 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.535+1034_535+1037d others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | ||||||
chr6:73467614 | A | AAAATAAA others(1): Show |
119 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(116): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.535+1030_535+1037d others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | ||||||
chr6:73467614 | A | AAAATAAA others(5): Show |
52 | a0001c0001t0006g0187 a0001c0001t0006g0188 a0001c0001t0006g0191 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.535+1026_535+1037d others(14): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | ||||||
chr6:73467614 | A | AAAATAAA others(9): Show |
27 | a0001c0001t0006g0249 a0001c0001t0025g0141 a0001c0001t0025g0142 others(24): Show |
27 | HG01070.hp2 HG01099.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.535+1022_535+1037d others(18): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | ||||||
chr6:73467614 | A | AAAATAAA others(13): Show |
36 | a0001c0001t0025g0140 a0001c0002t0002g0025 a0001c0002t0002g0026 others(33): Show |
36 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.535+1018_535+1037d others(22): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | ||||||
chr6:73467614 | A | AAAATAAA others(17): Show |
5 | a0001c0002t0011g0022 a0001c0002t0011g0031 a0001c0002t0038g0030 others(2): Show |
5 | HG00438.hp2 HG01261.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+1014_535+1037d others(26): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | ||||||
chr6:73467615 | A | AAATAAAT others(12): Show |
1 | a0001c0001t0099g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.535+1012_535+1030d others(21): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467615 | ||||||
chr6:73467786 | G | A | 1 | a0001c0001t0100g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.535+1180G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467786 | |||||||
chr6:73467796 | T | C | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+1190T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467796 | |||||||
chr6:73467888 | T | A | 1 | a0001c0001t0078g0156 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.535+1282T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467888 | |||||||
chr6:73467924 | G | A | 13 | a0001c0002t0021g0071 a0001c0002t0021g0080 a0001c0002t0021g0087 others(10): Show |
13 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.535+1318G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467924 | |||||||
chr6:73467968 | G | A | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+1362G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467968 | |||||||
chr6:73468036 | G | A | 1 | a0002c0009t0010g0276 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.535+1430G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468036 | |||||||
chr6:73468043 | T | A | 1 | a0001c0001t0003g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.535+1437T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468043 | |||||||
chr6:73468065 | C | T | 21 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(18): Show |
21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.535+1459C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468065 | |||||||
chr6:73468108 | C | T | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+1502C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468108 | |||||||
chr6:73468143 | A | G | 4 | a0001c0002t0021g0087 a0001c0002t0021g0089 a0001c0002t0125g0086 others(1): Show |
4 | HG02572.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+1537A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468143 | |||||||
chr6:73468224 | T | C | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.535+1618T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468224 | |||||||
chr6:73468321 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.535+1715G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468321 | |||||||
chr6:73468365 | C | T | 2 | a0001c0001t0010g0302 a0001c0001t0010g0303 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.535+1759C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468365 | |||||||
chr6:73468397 | G | C | 1 | a0001c0002t0021g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.535+1791G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468397 | |||||||
chr6:73468673 | T | C | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+2067T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468673 | |||||||
chr6:73468851 | G | A | 11 | a0001c0001t0008g0019 a0001c0001t0008g0120 a0001c0001t0008g0121 others(8): Show |
11 | HG02040.hp2 HG02055.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.535+2245G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468851 | |||||||
chr6:73468917 | T | C | 1 | a0001c0001t0070g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.535+2311T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468917 | |||||||
chr6:73468989 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.535+2383T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468989 | |||||||
chr6:73469001 | T | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0311 a0001c0001t0007g0145 others(7): Show |
10 | HG00597.hp1 HG02074.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.535+2395T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469001 | |||||||
chr6:73469123 | A | G | 1 | a0001c0002t0002g0027 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.535+2517A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469123 | |||||||
chr6:73469191 | C | T | 14 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(11): Show |
14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.535+2585C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469191 | |||||||
chr6:73469192 | G | C | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+2586G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469192 | |||||||
chr6:73469377 | C | T | 1 | a0001c0001t0004g0210 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.535+2771C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469377 | |||||||
chr6:73469440 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.535+2834A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469440 | |||||||
chr6:73469441 | T | C | 14 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(11): Show |
14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.535+2835T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469441 | |||||||
chr6:73469483 | G | A | 8 | a0001c0001t0004g0200 a0001c0001t0004g0277 a0001c0001t0004g0278 others(5): Show |
8 | HG00639.hp2 HG00735.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.535+2877G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469483 | |||||||
chr6:73469499 | G | C | 8 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+2893G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469499 | |||||||
chr6:73469529 | A | G | 1 | a0001c0001t0032g0323 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.535+2923A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469529 | |||||||
chr6:73469536 | C | T | 1 | a0001c0001t0006g0267 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.535+2930C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469536 | |||||||
chr6:73469598 | G | A | 1 | a0001c0001t0007g0196 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.535+2992G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469598 | |||||||
chr6:73469650 | CT | C | 336 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(333): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.535+3046delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73469650 | ||||||
chr6:73469672 | A | G | 81 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(78): Show |
81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.535+3066A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469672 | |||||||
chr6:73469803 | G | C | 81 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(78): Show |
81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.535+3197G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469803 | |||||||
chr6:73469890 | A | C | 11 | a0001c0002t0021g0071 a0001c0002t0021g0080 a0001c0002t0021g0087 others(8): Show |
11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.535+3284A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469890 | |||||||
chr6:73469965 | A | T | 19 | a0001c0001t0001g0136 a0001c0001t0001g0178 a0001c0001t0001g0182 others(16): Show |
20 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.535+3359A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469965 | |||||||
chr6:73470053 | A | G | 2 | a0001c0001t0013g0183 a0001c0001t0013g0184 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.536-3312A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470053 | |||||||
chr6:73470065 | G | A | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.536-3300G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470065 | |||||||
chr6:73470084 | A | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0130 a0001c0001t0001g0131 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.536-3281A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470084 | |||||||
chr6:73470202 | A | AT | 4 | a0001c0001t0018g0144 a0001c0001t0018g0147 a0001c0001t0018g0159 others(1): Show |
4 | HG00597.hp1 HG02074.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-3157dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73470202 | ||||||
chr6:73470261 | C | T | 1 | a0001c0002t0116g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.536-3104C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470261 | |||||||
chr6:73470268 | G | C | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.536-3097G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470268 | |||||||
chr6:73470302 | G | A | 1 | a0001c0001t0008g0331 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.536-3063G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470302 | |||||||
chr6:73470310 | G | A | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.536-3055G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470310 | |||||||
chr6:73470345 | T | C | 8 | a0001c0001t0003g0106 a0001c0001t0003g0117 a0001c0001t0003g0118 others(5): Show |
8 | HG02004.hp2 HG02273.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.536-3020T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470345 | |||||||
chr6:73470393 | A | G | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.536-2972A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470393 | |||||||
chr6:73470453 | A | G | 3 | a0001c0002t0002g0052 a0001c0002t0002g0053 a0001c0002t0011g0029 |
3 | HG02056.hp1 NA18987.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.536-2912A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470453 | |||||||
chr6:73470469 | G | A | 3 | a0001c0001t0025g0140 a0001c0001t0025g0141 a0001c0001t0025g0142 |
3 | HG02622.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.536-2896G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470469 | |||||||
chr6:73470474 | G | A | 1 | a0001c0001t0049g0342 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.536-2891G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470474 | |||||||
chr6:73470479 | T | C | 1 | a0001c0001t0004g0201 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.536-2886T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470479 | |||||||
chr6:73470498 | G | A | 8 | a0001c0001t0015g0013 a0001c0001t0015g0286 a0001c0001t0015g0287 others(5): Show |
8 | HG00408.hp2 NA18612.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.536-2867G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470498 | |||||||
chr6:73470500 | G | A | 2 | a0001c0001t0010g0302 a0001c0001t0010g0303 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.536-2865G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470500 | |||||||
chr6:73470530 | A | G | 1 | a0001c0001t0061g0301 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.536-2835A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470530 | |||||||
chr6:73470620 | C | G | 3 | a0001c0001t0025g0140 a0001c0001t0025g0141 a0001c0001t0025g0142 |
3 | HG02622.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.536-2745C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470620 | |||||||
chr6:73470689 | C | G | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.536-2676C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470689 | |||||||
chr6:73470881 | A | T | 11 | a0001c0002t0021g0071 a0001c0002t0021g0080 a0001c0002t0021g0087 others(8): Show |
11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.536-2484A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470881 | |||||||
chr6:73470918 | A | T | 1 | a0001c0001t0025g0140 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.536-2447A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470918 | |||||||
chr6:73471006 | A | T | 1 | a0001c0001t0098g0320 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.536-2359A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471006 | |||||||
chr6:73471086 | A | G | 21 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(18): Show |
21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.536-2279A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471086 | |||||||
chr6:73471121 | C | T | 21 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(18): Show |
21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.536-2244C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471121 | |||||||
chr6:73471122 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.536-2243G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471122 | |||||||
chr6:73471206 | C | CT | 318 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(315): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.536-2148dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73471206 | ||||||
chr6:73471252 | A | G | 14 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(11): Show |
14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.536-2113A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471252 | |||||||
chr6:73471471 | G | A | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.536-1894G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471471 | |||||||
chr6:73471658 | T | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.536-1707T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471658 | |||||||
chr6:73471681 | G | T | 2 | a0001c0002t0021g0071 a0001c0002t0021g0080 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.536-1684G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471681 | |||||||
chr6:73471717 | C | T | 1 | a0001c0001t0046g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.536-1648C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471717 | |||||||
chr6:73471718 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0007g0196 a0001c0001t0007g0313 |
3 | HG02280.hp1 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.536-1647G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471718 | |||||||
chr6:73471771 | G | A | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.536-1594G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471771 | |||||||
chr6:73471818 | ATG | A | 57 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.536-1545_536-1544d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73471818 | ||||||
chr6:73471856 | G | A | 57 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.536-1509G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471856 | |||||||
chr6:73471899 | C | T | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.536-1466C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471899 | |||||||
chr6:73472009 | TG | T | 198 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(195): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.536-1355delG | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472009 | |||||||
chr6:73472027 | G | A | 57 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.536-1338G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472027 | |||||||
chr6:73472127 | G | A | 2 | a0001c0002t0011g0054 a0001c0002t0038g0032 |
2 | HG01070.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.536-1238G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472127 | |||||||
chr6:73472159 | T | C | 1 | a0001c0001t0045g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.536-1206T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472159 | |||||||
chr6:73472202 | G | A | 1 | a0001c0002t0002g0055 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.536-1163G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472202 | |||||||
chr6:73472425 | GACTA | G | 5 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0009g0128 others(2): Show |
5 | HG00741.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.536-936_536-933del others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73472425 | ||||||
chr6:73472525 | A | G | 2 | a0001c0002t0121g0081 a0001c0002t0122g0085 |
2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.536-840A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472525 | |||||||
chr6:73472716 | C | CA | 151 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(148): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.536-648dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73472716 | ||||||
chr6:73472729 | G | A | 1 | a0001c0001t0046g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.536-636G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472729 | |||||||
chr6:73472843 | A | G | 21 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(18): Show |
21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.536-522A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472843 | |||||||
chr6:73472939 | G | A | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.536-426G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472939 | |||||||
chr6:73473003 | C | T | 2 | a0001c0002t0121g0081 a0001c0002t0122g0085 |
2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.536-362C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73473003 | |||||||
chr6:73473182 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.536-183G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73473182 | |||||||
chr6:73473210 | C | T | 1 | a0001c0001t0070g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.536-155C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73473210 | |||||||
chr6:73473277 | C | CAGAT | 22 | a0001c0001t0001g0136 a0001c0001t0001g0178 a0001c0001t0004g0300 others(19): Show |
23 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.536-66_536-63dupGA others(2): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73473277 | ||||||
chr6:73473277 | C | CAGATAGA others(5): Show |
1 | a0001c0001t0001g0182 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.536-74_536-63dupGA others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73473277 | ||||||
chr6:73473277 | CAGAT | C | 8 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.536-66_536-63delGA others(2): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73473277 | ||||||
chr6:73473721 | C | CT | 291 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0131 others(288): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.825+84dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73473721 | ||||||
chr6:73473761 | C | G | 1 | a0001c0002t0122g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.825+107C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73473761 | |||||||
chr6:73473768 | T | C | 1 | a0001c0001t0084g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.825+114T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73473768 | |||||||
chr6:73473786 | A | AT | 30 | a0001c0001t0001g0245 a0001c0001t0001g0275 a0001c0001t0003g0002 others(27): Show |
32 | HG00438.hp1 HG00544.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.825+150dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73473786 | ||||||
chr6:73473786 | AT | A | 73 | a0001c0001t0013g0176 a0001c0001t0016g0094 a0001c0001t0016g0185 others(70): Show |
73 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.825+150delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73473786 | ||||||
chr6:73473861 | A | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0172 a0001c0001t0001g0239 others(4): Show |
9 | HG02129.hp1 NA18939.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.825+207A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73473861 | |||||||
chr6:73474098 | C | CT | 8 | a0001c0001t0004g0210 a0001c0001t0005g0356 a0001c0001t0010g0016 others(5): Show |
9 | HG01123.hp1 HG01346.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.825+456dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73474098 | ||||||
chr6:73474112 | T | A | 81 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(78): Show |
81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.825+458T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474112 | |||||||
chr6:73474592 | G | T | 3 | a0001c0001t0003g0104 a0001c0001t0003g0113 a0001c0001t0003g0114 |
3 | NA18980.hp1 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.825+938G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474592 | |||||||
chr6:73474593 | C | T | 3 | a0001c0001t0003g0104 a0001c0001t0003g0113 a0001c0001t0003g0114 |
3 | NA18980.hp1 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.825+939C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474593 | |||||||
chr6:73474594 | A | C | 1 | a0001c0001t0009g0310 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.825+940A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474594 | |||||||
chr6:73474594 | ACCC | A | 3 | a0001c0001t0003g0104 a0001c0001t0003g0113 a0001c0001t0003g0114 |
3 | NA18980.hp1 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.825+941_825+943del others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474594 | |||||||
chr6:73474691 | G | A | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.825+1037G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474691 | |||||||
chr6:73474752 | CT | C | 57 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.825+1110delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73474752 | ||||||
chr6:73474777 | C | T | 1 | a0001c0001t0004g0201 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.825+1123C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474777 | |||||||
chr6:73474786 | G | A | 4 | a0001c0002t0021g0087 a0001c0002t0021g0089 a0001c0002t0125g0086 others(1): Show |
4 | HG02572.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.825+1132G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474786 | |||||||
chr6:73474812 | A | G | 5 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.825+1158A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474812 | |||||||
chr6:73474817 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.825+1163G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474817 | |||||||
chr6:73474856 | A | G | 1 | a0001c0001t0007g0155 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.825+1202A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474856 | |||||||
chr6:73474907 | C | T | 1 | a0001c0001t0006g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.825+1253C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474907 | |||||||
chr6:73475114 | A | G | 1 | a0001c0001t0013g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.825+1460A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475114 | |||||||
chr6:73475183 | G | C | 1 | a0001c0001t0045g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.825+1529G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475183 | |||||||
chr6:73475249 | G | A | 8 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.825+1595G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475249 | |||||||
chr6:73475259 | G | T | 1 | a0001c0001t0007g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.825+1605G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475259 | |||||||
chr6:73475369 | G | A | 1 | a0001c0001t0006g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.825+1715G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475369 | |||||||
chr6:73475434 | C | T | 3 | a0001c0002t0002g0050 a0001c0002t0002g0066 a0001c0002t0011g0061 |
3 | NA18959.hp1 NA18981.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.825+1780C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475434 | |||||||
chr6:73475496 | A | G | 7 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(4): Show |
7 | HG03209.hp2 NA18946.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.825+1842A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475496 | |||||||
chr6:73475512 | C | CT | 11 | a0001c0001t0009g0238 a0001c0001t0024g0264 a0001c0001t0085g0171 others(8): Show |
11 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.825+1873dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73475512 | ||||||
chr6:73475528 | C | T | 1 | a0004c0005t0026g0028 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.825+1874C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475528 | |||||||
chr6:73475529 | T | C | 1 | a0004c0005t0026g0028 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.825+1875T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475529 | |||||||
chr6:73475567 | C | T | 14 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(11): Show |
14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.825+1913C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475567 | |||||||
chr6:73475627 | G | A | 2 | a0001c0002t0121g0081 a0001c0002t0122g0085 |
2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.825+1973G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475627 | |||||||
chr6:73475659 | C | T | 1 | a0001c0001t0006g0249 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.825+2005C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475659 | |||||||
chr6:73475687 | T | C | 2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.825+2033T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475687 | |||||||
chr6:73475702 | G | C | 1 | a0001c0001t0017g0358 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.825+2048G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475702 | |||||||
chr6:73475751 | A | T | 1 | a0001c0001t0071g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.825+2097A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475751 | |||||||
chr6:73475758 | C | T | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.825+2104C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475758 | |||||||
chr6:73475764 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.825+2110G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475764 | |||||||
chr6:73475793 | T | G | 2 | a0001c0001t0010g0302 a0001c0001t0010g0303 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.825+2139T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475793 | |||||||
chr6:73475826 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.825+2172G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475826 | |||||||
chr6:73475944 | C | T | 1 | a0001c0001t0009g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.825+2290C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475944 | |||||||
chr6:73475947 | C | A | 1 | a0001c0001t0008g0347 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.825+2293C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475947 | |||||||
chr6:73475965 | A | G | 1 | a0001c0002t0122g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.825+2311A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475965 | |||||||
chr6:73476088 | C | T | 2 | a0001c0001t0001g0311 a0001c0001t0007g0146 |
2 | NA19001.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.825+2434C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476088 | |||||||
chr6:73476134 | A | G | 338 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.825+2480A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476134 | |||||||
chr6:73476203 | A | AAATAAAA others(7): Show |
57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.825+2552_825+2565d others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476203 | ||||||
chr6:73476222 | A | C | 11 | a0001c0002t0021g0071 a0001c0002t0021g0080 a0001c0002t0021g0087 others(8): Show |
11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.825+2568A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476222 | |||||||
chr6:73476285 | A | G | 3 | a0001c0001t0008g0120 a0001c0001t0008g0121 a0001c0001t0008g0122 |
3 | HG02040.hp2 HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.825+2631A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476285 | |||||||
chr6:73476378 | C | CA | 11 | a0001c0001t0004g0203 a0001c0001t0008g0347 a0001c0001t0016g0094 others(8): Show |
11 | HG00280.hp1 HG00673.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.825+2743dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476378 | ||||||
chr6:73476378 | CA | C | 59 | a0001c0001t0001g0243 a0001c0001t0003g0118 a0001c0001t0005g0353 others(56): Show |
59 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.825+2743delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476378 | ||||||
chr6:73476378 | CAA | C | 23 | a0001c0002t0002g0049 a0001c0002t0002g0053 a0001c0002t0020g0072 others(20): Show |
23 | HG01515.hp2 HG01884.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.825+2742_825+2743d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476378 | ||||||
chr6:73476440 | G | A | 1 | a0001c0002t0120g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.825+2786G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476440 | |||||||
chr6:73476452 | A | AAAG | 80 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(77): Show |
80 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.825+2800_825+2801i others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476452 | ||||||
chr6:73476572 | G | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0035g0135 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.825+2918G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476572 | |||||||
chr6:73476739 | C | A | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.826-2993C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476739 | |||||||
chr6:73476790 | A | AT | 18 | a0001c0001t0016g0093 a0001c0001t0016g0185 a0001c0001t0016g0186 others(15): Show |
18 | HG02572.hp2 HG02622.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.826-2926dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476790 | ||||||
chr6:73476790 | AT | A | 9 | a0001c0001t0003g0118 a0001c0001t0006g0251 a0001c0001t0058g0289 others(6): Show |
9 | HG01109.hp2 HG01256.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.826-2926delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476790 | ||||||
chr6:73476812 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.826-2920G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476812 | |||||||
chr6:73476912 | T | G | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.826-2820T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476912 | |||||||
chr6:73476920 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.826-2812C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476920 | |||||||
chr6:73476943 | A | G | 1 | a0001c0001t0005g0363 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.826-2789A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476943 | |||||||
chr6:73477079 | G | A | 1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826-2653G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477079 | |||||||
chr6:73477093 | T | A | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.826-2639T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477093 | |||||||
chr6:73477257 | A | G | 338 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.826-2475A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477257 | |||||||
chr6:73477393 | CA | C | 181 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(178): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.826-2317delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73477393 | ||||||
chr6:73477393 | CAA | C | 143 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(140): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.826-2318_826-2317d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73477393 | ||||||
chr6:73477395 | A | AAAAAAAA others(844): Show |
1 | a0001c0001t0001g0158 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.826-2319_826-2318i others(853): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73477395 | ||||||
chr6:73477411 | A | G | 1 | a0001c0001t0098g0320 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.826-2321A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477411 | |||||||
chr6:73477509 | C | CT | 17 | a0001c0001t0001g0236 a0001c0001t0008g0341 a0001c0001t0014g0298 others(14): Show |
17 | HG00621.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.826-2208dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73477509 | ||||||
chr6:73477633 | A | G | 1 | a0001c0002t0002g0069 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.826-2099A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477633 | |||||||
chr6:73477767 | A | G | 22 | a0001c0002t0002g0026 a0001c0002t0002g0027 a0001c0002t0002g0041 others(19): Show |
22 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.826-1965A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477767 | |||||||
chr6:73477799 | G | A | 1 | a0001c0001t0098g0320 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.826-1933G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477799 | |||||||
chr6:73477817 | T | G | 1 | a0001c0002t0021g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.826-1915T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477817 | |||||||
chr6:73477848 | G | A | 1 | a0001c0001t0045g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.826-1884G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477848 | |||||||
chr6:73477944 | T | C | 1 | a0001c0001t0012g0220 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.826-1788T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477944 | |||||||
chr6:73478108 | G | A | 1 | a0001c0002t0002g0025 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.826-1624G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478108 | |||||||
chr6:73478244 | CA | C | 71 | a0001c0001t0032g0297 a0001c0002t0002g0006 a0001c0002t0002g0025 others(68): Show |
71 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.826-1472delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73478244 | ||||||
chr6:73478345 | C | A | 1 | a0002c0009t0010g0276 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.826-1387C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478345 | |||||||
chr6:73478347 | A | G | 2 | a0001c0001t0008g0331 a0001c0001t0048g0340 |
2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.826-1385A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478347 | |||||||
chr6:73478416 | C | CA | 63 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(60): Show |
65 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.826-1306dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73478416 | ||||||
chr6:73478482 | T | G | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.826-1250T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478482 | |||||||
chr6:73478629 | C | G | 1 | a0001c0002t0027g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.826-1103C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478629 | |||||||
chr6:73478789 | A | G | 342 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(339): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.826-943A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478789 | |||||||
chr6:73478880 | CT | C | 57 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.826-841delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73478880 | ||||||
chr6:73478901 | T | C | 3 | a0001c0001t0006g0188 a0001c0001t0006g0252 a0001c0001t0088g0189 |
3 | HG01515.hp1 HG01517.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.826-831T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478901 | |||||||
chr6:73478942 | G | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0270 a0001c0001t0009g0198 |
3 | HG02109.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.826-790G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478942 | |||||||
chr6:73479029 | C | T | 1 | a0001c0001t0009g0305 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.826-703C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479029 | |||||||
chr6:73479202 | A | C | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0009g0305 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.826-530A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479202 | |||||||
chr6:73479409 | C | T | 1 | a0001c0001t0013g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.826-323C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479409 | |||||||
chr6:73479451 | C | T | 1 | a0001c0001t0004g0201 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.826-281C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479451 | |||||||
chr6:73479490 | G | A | 1 | a0001c0001t0007g0145 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.826-242G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479490 | |||||||
chr6:73480227 | G | T | 1 | a0001c0001t0007g0196 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1129+101G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480227 | |||||||
chr6:73480265 | T | G | 1 | a0001c0001t0092g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1129+139T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480265 | |||||||
chr6:73480517 | G | A | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1130-158G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480517 | |||||||
chr6:73480528 | C | G | 3 | a0001c0001t0034g0138 a0001c0001t0034g0149 a0001c0001t0065g0152 |
3 | HG00280.hp1 HG01358.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1130-147C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480528 | |||||||
chr6:73480548 | G | A | 1 | a0003c0008t0001g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1130-127G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480548 | |||||||
chr6:73480904 | A | G | 1 | a0001c0001t0053g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1260+99A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73480904 | |||||||
chr6:73480969 | GT | G | 46 | a0001c0001t0001g0130 a0001c0001t0001g0199 a0001c0001t0001g0234 others(43): Show |
47 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1260+188delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | ||||||
chr6:73480969 | GTT | G | 188 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0131 others(185): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1260+187_1260+188d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | ||||||
chr6:73480969 | GTTT | G | 31 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(28): Show |
36 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.1260+186_1260+188d others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | ||||||
chr6:73480969 | GTTTT | G | 17 | a0001c0002t0002g0026 a0001c0002t0002g0027 a0001c0002t0002g0060 others(14): Show |
17 | HG00438.hp2 HG01884.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1260+185_1260+188d others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | ||||||
chr6:73480969 | GTTTTT | G | 59 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0034 others(56): Show |
59 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.1260+184_1260+188d others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | ||||||
chr6:73480969 | GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0017g0337 a0001c0001t0017g0358 a0001c0001t0017g0362 |
3 | HG02970.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1260+179_1260+188d others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | ||||||
chr6:73481161 | C | T | 1 | a0001c0001t0075g0231 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1260+356C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481161 | |||||||
chr6:73481258 | A | G | 7 | a0001c0001t0008g0019 a0001c0001t0008g0331 a0001c0001t0008g0332 others(4): Show |
7 | HG02055.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+453A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481258 | |||||||
chr6:73481306 | G | C | 1 | a0001c0001t0004g0277 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1260+501G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481306 | |||||||
chr6:73481384 | A | G | 25 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(22): Show |
30 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+579A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481384 | |||||||
chr6:73481468 | TA | T | 377 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(374): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1261-564delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73481468 | ||||||
chr6:73481563 | C | T | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1261-477C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481563 | |||||||
chr6:73481733 | A | G | 4 | a0001c0002t0021g0087 a0001c0002t0021g0089 a0001c0002t0125g0086 others(1): Show |
4 | HG02572.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-307A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481733 | |||||||
chr6:73481822 | G | A | 342 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(339): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1261-218G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481822 | |||||||
chr6:73481864 | A | G | 1 | a0001c0001t0044g0357 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1261-176A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481864 | |||||||
chr6:73482296 | A | G | 2 | a0001c0001t0010g0302 a0001c0001t0010g0303 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1465+52A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 8/11 | chr6 | 73482296 | |||||||
chr6:73482415 | A | G | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1466-34A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 8/11 | chr6 | 73482415 | |||||||
chr6:73482679 | C | A | 8 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+59C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482679 | |||||||
chr6:73482699 | T | G | 57 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1637+79T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482699 | |||||||
chr6:73482789 | C | CT | 139 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(136): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1637+191dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | ||||||
chr6:73482789 | C | CTT | 106 | a0001c0001t0001g0199 a0001c0001t0001g0235 a0001c0001t0001g0236 others(103): Show |
111 | HG00621.hp1 HG00621.hp2 HG00733.hp2 others(108): Show |
intron_variant | MODIFIER | c.1637+190_1637+191d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | ||||||
chr6:73482789 | C | CTTT | 7 | a0001c0001t0003g0098 a0001c0002t0002g0038 a0001c0002t0002g0048 others(4): Show |
7 | HG00438.hp2 HG00597.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+189_1637+191d others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | ||||||
chr6:73482789 | CTT | C | 11 | a0001c0001t0001g0158 a0001c0001t0001g0311 a0001c0001t0007g0145 others(8): Show |
11 | HG00597.hp1 HG02074.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1637+190_1637+191d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | ||||||
chr6:73482789 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0005g0334 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1637+178_1637+191d others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | ||||||
chr6:73482793 | T | C | 1 | a0001c0001t0008g0341 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1637+173T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482793 | |||||||
chr6:73482822 | C | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(113): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1637+202C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482822 | |||||||
chr6:73482834 | C | T | 1 | a0001c0001t0087g0229 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1637+214C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482834 | |||||||
chr6:73482902 | C | A | 1 | a0001c0002t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1637+282C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482902 | |||||||
chr6:73482937 | G | A | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+317G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482937 | |||||||
chr6:73483002 | C | T | 11 | a0001c0002t0021g0071 a0001c0002t0021g0080 a0001c0002t0021g0087 others(8): Show |
11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+382C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483002 | |||||||
chr6:73483087 | C | T | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1637+467C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483087 | |||||||
chr6:73483183 | C | T | 1 | a0001c0001t0046g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1637+563C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483183 | |||||||
chr6:73483266 | G | A | 7 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(4): Show |
7 | HG03209.hp2 NA18946.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+646G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483266 | |||||||
chr6:73483331 | C | T | 11 | a0001c0002t0021g0071 a0001c0002t0021g0080 a0001c0002t0021g0087 others(8): Show |
11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+711C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483331 | |||||||
chr6:73483398 | C | T | 1 | a0001c0002t0002g0047 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1637+778C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483398 | |||||||
chr6:73483464 | A | T | 1 | a0001c0002t0011g0031 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1637+844A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483464 | |||||||
chr6:73483506 | A | G | 1 | a0001c0002t0122g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1637+886A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483506 | |||||||
chr6:73483654 | C | T | 5 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1637+1034C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483654 | |||||||
chr6:73483784 | A | AT | 43 | a0001c0001t0001g0234 a0001c0001t0003g0001 a0001c0001t0003g0002 others(40): Show |
48 | HG00544.hp1 HG00735.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1637+1184dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73483784 | ||||||
chr6:73483784 | AT | A | 90 | a0001c0001t0006g0259 a0001c0001t0007g0155 a0001c0001t0007g0232 others(87): Show |
90 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.1637+1184delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73483784 | ||||||
chr6:73483846 | T | C | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1637+1226T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483846 | |||||||
chr6:73483897 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1637+1277G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483897 | |||||||
chr6:73483939 | C | T | 1 | a0001c0001t0008g0332 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1637+1319C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483939 | |||||||
chr6:73484022 | A | G | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+1402A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484022 | |||||||
chr6:73484101 | T | C | 10 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(7): Show |
10 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1637+1481T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484101 | |||||||
chr6:73484146 | A | G | 1 | a0001c0001t0016g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1637+1526A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484146 | |||||||
chr6:73484173 | G | A | 1 | a0001c0001t0071g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1637+1553G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484173 | |||||||
chr6:73484234 | G | A | 2 | a0001c0001t0031g0348 a0001c0001t0031g0352 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1637+1614G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484234 | |||||||
chr6:73484394 | C | G | 2 | a0001c0002t0021g0071 a0001c0002t0021g0080 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1637+1774C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484394 | |||||||
chr6:73484483 | T | C | 14 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(11): Show |
14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1637+1863T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484483 | |||||||
chr6:73484488 | G | A | 1 | a0001c0001t0056g0321 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1637+1868G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484488 | |||||||
chr6:73484551 | CATT | C | 19 | a0001c0001t0001g0136 a0001c0001t0001g0178 a0001c0001t0001g0182 others(16): Show |
20 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1637+1933_1637+193 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73484551 | ||||||
chr6:73484783 | C | T | 81 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(78): Show |
81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1637+2163C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484783 | |||||||
chr6:73484858 | C | G | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1637+2238C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484858 | |||||||
chr6:73484936 | A | C | 1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1637+2316A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484936 | |||||||
chr6:73484938 | T | G | 2 | a0001c0001t0001g0163 a0001c0001t0007g0148 |
2 | HG00280.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1637+2318T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484938 | |||||||
chr6:73484940 | A | G | 1 | a0001c0001t0007g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1637+2320A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484940 | |||||||
chr6:73485014 | T | C | 1 | a0001c0001t0055g0291 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1637+2394T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485014 | |||||||
chr6:73485023 | C | T | 3 | a0001c0001t0004g0290 a0001c0001t0004g0300 a0001c0001t0032g0297 |
3 | NA18939.hp1 NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1637+2403C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485023 | |||||||
chr6:73485046 | C | CA | 60 | a0001c0001t0007g0313 a0001c0001t0008g0120 a0001c0001t0016g0093 others(57): Show |
60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1637+2443dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485046 | ||||||
chr6:73485046 | CA | C | 9 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0010g0302 others(6): Show |
9 | HG01109.hp2 HG02818.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1637+2443delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485046 | ||||||
chr6:73485106 | A | G | 1 | a0001c0001t0005g0360 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1637+2486A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485106 | |||||||
chr6:73485205 | A | G | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1637+2585A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485205 | |||||||
chr6:73485229 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1637+2609A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485229 | |||||||
chr6:73485436 | T | C | 3 | a0001c0001t0007g0233 a0001c0001t0036g0164 a0001c0001t0036g0174 |
3 | HG02071.hp1 NA19009.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1637+2816T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485436 | |||||||
chr6:73485441 | C | CT | 15 | a0001c0001t0001g0317 a0001c0001t0005g0350 a0001c0001t0005g0365 others(12): Show |
15 | HG01109.hp1 HG02257.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1637+2836dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485441 | ||||||
chr6:73485441 | C | CTTT | 10 | a0001c0002t0021g0071 a0001c0002t0021g0080 a0001c0002t0021g0087 others(7): Show |
10 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1637+2834_1637+283 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485441 | ||||||
chr6:73485441 | CT | C | 6 | a0001c0001t0001g0133 a0001c0001t0008g0347 a0001c0001t0061g0301 others(3): Show |
6 | HG01109.hp2 HG02818.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+2836delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485441 | ||||||
chr6:73485481 | T | C | 378 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(375): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1637+2861T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485481 | |||||||
chr6:73485583 | C | T | 1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1637+2963C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485583 | |||||||
chr6:73485589 | C | G | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+2969C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485589 | |||||||
chr6:73485611 | G | A | 1 | a0001c0001t0007g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1637+2991G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485611 | |||||||
chr6:73485736 | T | C | 338 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1637+3116T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485736 | |||||||
chr6:73485808 | C | T | 339 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(336): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1637+3188C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485808 | |||||||
chr6:73485925 | C | T | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+3305C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485925 | |||||||
chr6:73485932 | G | A | 81 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(78): Show |
81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1637+3312G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485932 | |||||||
chr6:73485940 | TACAC | T | 81 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(78): Show |
81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1637+3336_1637+333 others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485940 | ||||||
chr6:73485961 | T | C | 2 | a0001c0002t0021g0071 a0001c0002t0021g0080 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1637+3341T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485961 | |||||||
chr6:73486040 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1637+3420A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486040 | |||||||
chr6:73486113 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1637+3493A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486113 | |||||||
chr6:73486182 | A | C | 1 | a0001c0001t0035g0177 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1637+3562A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486182 | |||||||
chr6:73486258 | A | T | 257 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(254): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1637+3638A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486258 | |||||||
chr6:73486341 | A | G | 1 | a0001c0001t0084g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1637+3721A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486341 | |||||||
chr6:73486425 | CTATGGAT others(8): Show |
C | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1637+3806_1637+382 others(19): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486425 | |||||||
chr6:73486429 | G | A | 2 | a0001c0001t0010g0302 a0001c0001t0010g0303 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1637+3809G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486429 | |||||||
chr6:73486430 | G | T | 1 | a0001c0001t0046g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1637+3810G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486430 | |||||||
chr6:73486487 | C | G | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+3867C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486487 | |||||||
chr6:73486496 | A | G | 342 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(339): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1637+3876A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486496 | |||||||
chr6:73486567 | G | A | 15 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0214 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1637+3947G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486567 | |||||||
chr6:73486641 | G | A | 1 | a0001c0001t0009g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1637+4021G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486641 | |||||||
chr6:73486766 | G | A | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+4146G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486766 | |||||||
chr6:73486784 | T | C | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+4164T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486784 | |||||||
chr6:73486880 | C | G | 57 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1637+4260C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486880 | |||||||
chr6:73487011 | G | GGAT | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+4392_1637+439 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487011 | ||||||
chr6:73487096 | C | G | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1637+4476C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487096 | |||||||
chr6:73487151 | G | A | 1 | a0001c0002t0002g0057 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1637+4531G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487151 | |||||||
chr6:73487197 | AT | A | 284 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(281): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1637+4597delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487197 | ||||||
chr6:73487197 | ATT | A | 21 | a0001c0001t0001g0325 a0001c0001t0004g0277 a0001c0001t0006g0251 others(18): Show |
21 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1637+4596_1637+459 others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487197 | ||||||
chr6:73487197 | ATTT | A | 53 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(50): Show |
53 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1637+4595_1637+459 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487197 | ||||||
chr6:73487249 | G | C | 14 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(11): Show |
14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1637+4629G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487249 | |||||||
chr6:73487556 | G | GT | 40 | a0001c0001t0001g0309 a0001c0001t0005g0018 a0001c0001t0005g0020 others(37): Show |
43 | HG00438.hp2 HG00642.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1638-4662dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487556 | ||||||
chr6:73487556 | GT | G | 55 | a0001c0001t0001g0178 a0001c0001t0003g0001 a0001c0001t0003g0002 others(52): Show |
60 | HG00544.hp2 HG00735.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.1638-4662delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487556 | ||||||
chr6:73487577 | G | GT | 34 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(31): Show |
39 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1638-4645dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487577 | ||||||
chr6:73487604 | G | A | 1 | a0001c0001t0012g0220 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1638-4630G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487604 | |||||||
chr6:73487792 | C | T | 1 | a0001c0002t0011g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1638-4442C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487792 | |||||||
chr6:73487809 | G | A | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1638-4425G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487809 | |||||||
chr6:73487825 | C | T | 55 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(52): Show |
55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1638-4409C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487825 | |||||||
chr6:73487938 | G | A | 79 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(76): Show |
79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1638-4296G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487938 | |||||||
chr6:73487947 | A | G | 2 | a0001c0001t0073g0161 a0001c0001t0094g0166 |
2 | HG00140.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1638-4287A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487947 | |||||||
chr6:73488232 | G | T | 19 | a0001c0001t0001g0136 a0001c0001t0001g0178 a0001c0001t0001g0182 others(16): Show |
20 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1638-4002G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488232 | |||||||
chr6:73488452 | C | T | 1 | a0001c0002t0002g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1638-3782C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488452 | |||||||
chr6:73488554 | C | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0199 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1638-3680C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488554 | |||||||
chr6:73488572 | T | C | 1 | a0001c0002t0020g0078 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1638-3662T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488572 | |||||||
chr6:73488618 | A | T | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1638-3616A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488618 | |||||||
chr6:73488814 | G | A | 1 | a0001c0001t0046g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1638-3420G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488814 | |||||||
chr6:73488956 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1638-3278C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488956 | |||||||
chr6:73489077 | C | A | 4 | a0001c0001t0017g0337 a0001c0001t0017g0358 a0001c0001t0017g0361 others(1): Show |
4 | HG02970.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-3157C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489077 | |||||||
chr6:73489125 | A | G | 5 | a0001c0002t0029g0007 a0001c0002t0029g0083 a0001c0002t0029g0084 others(2): Show |
5 | HG02165.hp1 NA18969.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-3109A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489125 | |||||||
chr6:73489278 | C | CT | 186 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(183): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1638-2944dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73489278 | ||||||
chr6:73489278 | CT | C | 13 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(10): Show |
16 | HG01496.hp1 HG01978.hp1 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.1638-2944delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73489278 | ||||||
chr6:73489285 | T | C | 1 | a0001c0002t0011g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1638-2949T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489285 | |||||||
chr6:73489442 | C | G | 1 | a0001c0001t0009g0127 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1638-2792C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489442 | |||||||
chr6:73489619 | C | A | 2 | a0001c0001t0010g0302 a0001c0001t0010g0303 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1638-2615C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489619 | |||||||
chr6:73489720 | A | G | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1638-2514A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489720 | |||||||
chr6:73489724 | T | A | 6 | a0001c0001t0009g0126 a0001c0001t0009g0127 a0001c0001t0009g0128 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-2510T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489724 | |||||||
chr6:73489760 | C | A | 1 | a0001c0001t0006g0195 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1638-2474C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489760 | |||||||
chr6:73489795 | G | A | 200 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(197): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1638-2439G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489795 | |||||||
chr6:73490051 | A | G | 8 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-2183A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490051 | |||||||
chr6:73490076 | G | A | 338 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1638-2158G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490076 | |||||||
chr6:73490376 | C | T | 5 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0367 others(2): Show |
5 | NA18946.hp2 NA18957.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-1858C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490376 | |||||||
chr6:73490383 | G | C | 57 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1638-1851G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490383 | |||||||
chr6:73490464 | TG | T | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1638-1769delG | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490464 | |||||||
chr6:73490545 | A | G | 1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1638-1689A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490545 | |||||||
chr6:73490680 | C | T | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1638-1554C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490680 | |||||||
chr6:73490723 | T | TA | 82 | a0001c0001t0001g0269 a0001c0001t0001g0307 a0001c0001t0076g0271 others(79): Show |
82 | HG00438.hp2 HG00597.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.1638-1500dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73490723 | ||||||
chr6:73490752 | C | T | 1 | a0001c0002t0002g0055 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1638-1482C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490752 | |||||||
chr6:73490934 | A | C | 10 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(7): Show |
10 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1638-1300A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490934 | |||||||
chr6:73490940 | A | G | 2 | a0001c0001t0024g0257 a0001c0001t0024g0258 |
2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1638-1294A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490940 | |||||||
chr6:73491003 | A | G | 150 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(147): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1638-1231A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491003 | |||||||
chr6:73491118 | A | G | 1 | a0001c0002t0123g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1638-1116A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491118 | |||||||
chr6:73491122 | A | C | 2 | a0001c0002t0002g0044 a0001c0002t0002g0051 |
2 | NA18941.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1638-1112A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491122 | |||||||
chr6:73491246 | T | G | 14 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(11): Show |
14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1638-988T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491246 | |||||||
chr6:73491266 | GA | G | 335 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(332): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1638-954delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73491266 | ||||||
chr6:73491307 | G | A | 2 | a0001c0001t0031g0348 a0001c0001t0031g0352 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1638-927G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491307 | |||||||
chr6:73491357 | C | T | 2 | a0001c0001t0004g0015 a0001c0001t0057g0295 |
3 | NA18962.hp2 NA18974.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1638-877C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491357 | |||||||
chr6:73491361 | G | C | 33 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(30): Show |
38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1638-873G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491361 | |||||||
chr6:73491396 | C | CA | 70 | a0001c0001t0003g0109 a0001c0001t0004g0014 a0001c0001t0004g0015 others(67): Show |
72 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1638-821dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73491396 | ||||||
chr6:73491408 | A | G | 1 | a0001c0003t0030g0355 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1638-826A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491408 | |||||||
chr6:73491411 | A | AG | 11 | a0001c0001t0001g0158 a0001c0001t0001g0311 a0001c0001t0007g0145 others(8): Show |
11 | HG00597.hp1 HG02074.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1638-823_1638-822i others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491411 | |||||||
chr6:73491411 | A | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(139): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1638-823A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491411 | |||||||
chr6:73491558 | G | A | 1 | a0001c0002t0029g0084 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1638-676G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491558 | |||||||
chr6:73491703 | A | G | 1 | a0001c0002t0114g0033 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1638-531A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491703 | |||||||
chr6:73491878 | A | G | 338 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1638-356A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491878 | |||||||
chr6:73491915 | G | A | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1638-319G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491915 | |||||||
chr6:73491947 | A | C | 1 | a0001c0001t0045g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1638-287A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491947 | |||||||
chr6:73491953 | A | T | 338 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1638-281A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491953 | |||||||
chr6:73492010 | G | A | 1 | a0001c0002t0002g0026 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1638-224G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73492010 | |||||||
chr6:73492090 | C | T | 185 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(182): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1638-144C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73492090 | |||||||
chr6:73492103 | CA | C | 235 | a0001c0001t0001g0012 a0001c0001t0001g0130 a0001c0001t0001g0131 others(232): Show |
242 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.1638-116delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73492103 | ||||||
chr6:73492103 | CAA | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0158 others(103): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1638-117_1638-116d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73492103 | ||||||
chr6:73492169 | C | T | 1 | a0001c0001t0009g0238 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1638-65C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73492169 | |||||||
chr6:73492194 | C | T | 2 | a0001c0001t0014g0205 a0001c0001t0014g0288 |
2 | NA18944.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1638-40C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73492194 | |||||||
chr6:73492437 | A | C | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1756+85A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492437 | |||||||
chr6:73492550 | T | C | 338 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1756+198T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492550 | |||||||
chr6:73492604 | A | G | 1 | a0001c0001t0015g0287 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1756+252A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492604 | |||||||
chr6:73492655 | T | C | 2 | a0001c0001t0040g0193 a0001c0001t0040g0261 |
2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1756+303T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492655 | |||||||
chr6:73492676 | G | A | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1756+324G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492676 | |||||||
chr6:73492708 | G | C | 2 | a0001c0002t0002g0035 a0001c0002t0002g0039 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1756+356G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492708 | |||||||
chr6:73492756 | T | C | 2 | a0001c0001t0036g0164 a0001c0001t0036g0174 |
2 | NA19009.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1756+404T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492756 | |||||||
chr6:73492801 | A | G | 186 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(183): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1756+449A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492801 | |||||||
chr6:73492806 | T | TA | 207 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(204): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1756+470dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492806 | ||||||
chr6:73492806 | T | TAA | 132 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(129): Show |
134 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.1756+469_1756+470d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492806 | ||||||
chr6:73492968 | A | ATGTG | 10 | a0001c0002t0021g0071 a0001c0002t0021g0080 a0001c0002t0021g0087 others(7): Show |
10 | HG01884.hp1 HG02080.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1756+638_1756+641d others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | ||||||
chr6:73492968 | A | ATGTGTG | 55 | a0001c0001t0017g0362 a0001c0001t0089g0248 a0001c0002t0002g0006 others(52): Show |
55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1756+636_1756+641d others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | ||||||
chr6:73492968 | A | ATGTGTGT others(1): Show |
68 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(65): Show |
70 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.1756+634_1756+641d others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | ||||||
chr6:73492968 | A | ATGTGTGT others(3): Show |
28 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(25): Show |
31 | HG00741.hp1 HG01074.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1756+632_1756+641d others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | ||||||
chr6:73492968 | A | ATGTGTGT others(5): Show |
12 | a0001c0001t0008g0019 a0001c0001t0008g0331 a0001c0001t0008g0338 others(9): Show |
12 | HG02055.hp1 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1756+630_1756+641d others(14): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | ||||||
chr6:73492968 | A | ATGTGTGT others(7): Show |
4 | a0001c0001t0005g0360 a0001c0001t0008g0339 a0001c0001t0017g0361 others(1): Show |
4 | HG02965.hp1 HG03017.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1756+628_1756+641d others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | ||||||
chr6:73492968 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1756+626_1756+641d others(18): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | ||||||
chr6:73492968 | A | G | 4 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 others(1): Show |
4 | HG01109.hp2 HG02818.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1756+616A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492968 | |||||||
chr6:73492992 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0053g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1756+641_1756+642i others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492992 | ||||||
chr6:73492993 | T | TGTGTGTG others(4): Show |
4 | a0001c0001t0016g0185 a0001c0001t0025g0140 a0001c0001t0025g0141 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1756+641_1756+642i others(13): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492993 | |||||||
chr6:73492993 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0016g0367 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1756+641_1756+642i others(15): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492993 | |||||||
chr6:73492994 | A | G | 189 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(186): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1756+642A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492994 | |||||||
chr6:73492994 | A | T | 12 | a0001c0001t0004g0277 a0001c0001t0004g0281 a0001c0001t0016g0185 others(9): Show |
12 | HG01106.hp2 HG01255.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1756+642A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492994 | |||||||
chr6:73492995 | T | TGTA | 3 | a0001c0001t0007g0233 a0001c0001t0036g0164 a0001c0001t0036g0174 |
3 | HG02071.hp1 NA19009.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1756+643_1756+644i others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | |||||||
chr6:73492995 | T | TGTGTA | 20 | a0001c0001t0001g0182 a0001c0001t0003g0001 a0001c0001t0003g0098 others(17): Show |
23 | HG02004.hp2 HG03491.hp2 HG03492.hp2 others(20): Show |
intron_variant | MODIFIER | c.1756+643_1756+644i others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | |||||||
chr6:73492995 | T | TGTGTGTA | 141 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0134 others(138): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1756+643_1756+644i others(9): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | |||||||
chr6:73492995 | T | TGTGTGTG others(2): Show |
20 | a0001c0001t0001g0012 a0001c0001t0001g0130 a0001c0001t0001g0131 others(17): Show |
21 | HG01168.hp2 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1756+643_1756+644i others(11): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | |||||||
chr6:73492995 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0007g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1756+643_1756+644i others(13): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | |||||||
chr6:73492995 | T | TGTGTGTG others(14): Show |
3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1756+643_1756+644i others(23): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | |||||||
chr6:73492996 | T | A | 1 | a0001c0001t0089g0248 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1756+644T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492996 | |||||||
chr6:73493035 | C | T | 186 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(183): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1756+683C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493035 | |||||||
chr6:73493087 | C | T | 11 | a0001c0002t0021g0071 a0001c0002t0021g0080 a0001c0002t0021g0087 others(8): Show |
11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1756+735C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493087 | |||||||
chr6:73493206 | G | A | 1 | a0001c0001t0006g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1756+854G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493206 | |||||||
chr6:73493350 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1756+998A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493350 | |||||||
chr6:73493354 | A | ATG | 137 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(134): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1756+1036_1756+103 others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | A | ATGTG | 27 | a0001c0001t0003g0106 a0001c0001t0003g0114 a0001c0001t0004g0278 others(24): Show |
27 | HG00621.hp2 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1756+1034_1756+103 others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | A | ATGTGTG | 17 | a0001c0001t0001g0012 a0001c0001t0001g0130 a0001c0001t0001g0131 others(14): Show |
18 | HG01884.hp2 HG02015.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1756+1032_1756+103 others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | A | ATGTGTGT others(1): Show |
31 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0158 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1756+1030_1756+103 others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | A | ATGTGTGT others(3): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0182 a0001c0001t0001g0230 others(14): Show |
19 | HG00438.hp1 HG00621.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1756+1028_1756+103 others(14): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | A | ATGTGTGT others(5): Show |
40 | a0001c0001t0001g0134 a0001c0001t0001g0170 a0001c0001t0001g0218 others(37): Show |
41 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1756+1026_1756+103 others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | A | ATGTGTGT others(7): Show |
11 | a0001c0001t0001g0172 a0001c0001t0001g0178 a0001c0001t0001g0242 others(8): Show |
11 | HG01516.hp1 HG01517.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.1756+1024_1756+103 others(18): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1756+1002A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493354 | |||||||
chr6:73493354 | ATG | A | 42 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(39): Show |
45 | HG00741.hp1 HG01074.hp2 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.1756+1036_1756+103 others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | ATGTG | A | 22 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0001c0001t0025g0140 others(19): Show |
22 | HG02165.hp1 HG02257.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.1756+1034_1756+103 others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | ATGTGTG | A | 10 | a0001c0001t0016g0094 a0001c0002t0021g0071 a0001c0002t0021g0080 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1756+1032_1756+103 others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493354 | ATGTGTGT others(7): Show |
A | 4 | a0001c0001t0014g0205 a0001c0001t0014g0288 a0001c0001t0014g0298 others(1): Show |
4 | NA18944.hp1 NA18973.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1756+1024_1756+103 others(18): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | ||||||
chr6:73493389 | T | TGTGTGTG others(2): Show |
3 | a0001c0001t0009g0310 a0001c0001t0083g0263 a0001c0001t0085g0171 |
3 | HG01192.hp1 NA18978.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1756+1037_1756+103 others(13): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493389 | |||||||
chr6:73493389 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0084g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1756+1037_1756+103 others(15): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493389 | |||||||
chr6:73493389 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0007g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1756+1037_1756+103 others(17): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493389 | |||||||
chr6:73493391 | T | G | 1 | a0001c0001t0083g0263 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1756+1039T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493391 | |||||||
chr6:73493638 | G | A | 1 | a0001c0001t0019g0100 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1756+1286G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493638 | |||||||
chr6:73493641 | T | C | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1756+1289T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493641 | |||||||
chr6:73493702 | A | G | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1756+1350A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493702 | |||||||
chr6:73493824 | C | T | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1756+1472C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493824 | |||||||
chr6:73493896 | G | A | 1 | a0001c0001t0007g0212 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1756+1544G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493896 | |||||||
chr6:73494012 | C | G | 1 | a0001c0002t0002g0038 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1756+1660C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494012 | |||||||
chr6:73494109 | C | T | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1756+1757C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494109 | |||||||
chr6:73494163 | A | G | 1 | a0001c0001t0015g0294 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1756+1811A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494163 | |||||||
chr6:73494436 | A | T | 1 | a0001c0001t0016g0093 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1756+2084A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494436 | |||||||
chr6:73494479 | C | CT | 15 | a0001c0001t0012g0123 a0001c0001t0016g0093 a0001c0001t0016g0094 others(12): Show |
15 | HG01175.hp1 HG02622.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.1756+2142dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73494479 | ||||||
chr6:73494479 | CT | C | 76 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(73): Show |
76 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1756+2142delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73494479 | ||||||
chr6:73494508 | G | A | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1756+2156G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494508 | |||||||
chr6:73494516 | G | C | 2 | a0001c0002t0011g0054 a0001c0002t0038g0032 |
2 | HG01070.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1756+2164G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494516 | |||||||
chr6:73494528 | T | C | 2 | a0001c0001t0024g0257 a0001c0001t0024g0258 |
2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1756+2176T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494528 | |||||||
chr6:73494538 | G | A | 1 | a0001c0001t0010g0016 | 2 | HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1756+2186G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494538 | |||||||
chr6:73494658 | G | A | 7 | a0001c0001t0016g0093 a0001c0001t0016g0094 a0001c0001t0016g0185 others(4): Show |
7 | HG03209.hp2 NA18946.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.1756+2306G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494658 | |||||||
chr6:73494723 | G | A | 10 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(7): Show |
10 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1756+2371G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494723 | |||||||
chr6:73494775 | C | CT | 79 | a0001c0001t0001g0218 a0001c0001t0001g0311 a0001c0001t0019g0100 others(76): Show |
79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1756+2437dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73494775 | ||||||
chr6:73494778 | T | C | 1 | a0001c0001t0015g0328 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1756+2426T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494778 | |||||||
chr6:73494928 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1756+2576C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494928 | |||||||
chr6:73495084 | A | G | 1 | a0001c0001t0046g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1757-2652A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495084 | |||||||
chr6:73495319 | G | A | 1 | a0001c0001t0005g0349 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1757-2417G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495319 | |||||||
chr6:73495402 | C | T | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1757-2334C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495402 | |||||||
chr6:73495597 | C | T | 5 | a0001c0002t0029g0007 a0001c0002t0029g0083 a0001c0002t0029g0084 others(2): Show |
5 | HG02165.hp1 NA18969.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757-2139C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495597 | |||||||
chr6:73495908 | G | A | 341 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(338): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1757-1828G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495908 | |||||||
chr6:73496035 | A | G | 1 | a0001c0001t0016g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1757-1701A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496035 | |||||||
chr6:73496038 | A | C | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1757-1698A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496038 | |||||||
chr6:73496129 | G | A | 1 | a0001c0001t0016g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1757-1607G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496129 | |||||||
chr6:73496233 | G | A | 1 | a0001c0001t0034g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1757-1503G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496233 | |||||||
chr6:73496285 | C | T | 2 | a0001c0002t0121g0081 a0001c0002t0122g0085 |
2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1757-1451C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496285 | |||||||
chr6:73496320 | T | C | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1757-1416T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496320 | |||||||
chr6:73496440 | T | A | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1757-1296T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496440 | |||||||
chr6:73496441 | A | T | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1757-1295A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496441 | |||||||
chr6:73496442 | T | C | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1757-1294T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496442 | |||||||
chr6:73496625 | A | AC | 11 | a0001c0001t0003g0111 a0001c0001t0005g0363 a0001c0001t0006g0187 others(8): Show |
11 | HG01175.hp1 HG01496.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1757-1106dupC | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73496625 | ||||||
chr6:73496625 | A | C | 1 | a0001c0001t0070g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1757-1111A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496625 | |||||||
chr6:73496631 | T | C | 4 | a0001c0001t0012g0244 a0001c0001t0032g0323 a0001c0001t0048g0340 others(1): Show |
4 | HG01978.hp2 HG02055.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1757-1105T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496631 | |||||||
chr6:73496631 | T | TC | 7 | a0001c0001t0025g0142 a0001c0001t0034g0138 a0001c0001t0058g0289 others(4): Show |
7 | HG01358.hp2 HG01928.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1757-1099dupC | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73496631 | ||||||
chr6:73496632 | C | T | 1 | a0004c0005t0026g0028 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1757-1104C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496632 | |||||||
chr6:73496776 | C | T | 3 | a0001c0001t0004g0280 a0001c0001t0004g0281 a0001c0001t0004g0282 |
3 | HG00639.hp2 HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1757-960C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496776 | |||||||
chr6:73496778 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1757-958G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496778 | |||||||
chr6:73496781 | A | G | 1 | a0001c0001t0042g0364 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1757-955A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496781 | |||||||
chr6:73496886 | C | A | 1 | a0001c0002t0029g0083 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1757-850C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496886 | |||||||
chr6:73496913 | C | T | 4 | a0001c0001t0017g0337 a0001c0001t0017g0358 a0001c0001t0017g0361 others(1): Show |
4 | HG02970.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1757-823C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496913 | |||||||
chr6:73496914 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0009g0305 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1757-822G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496914 | |||||||
chr6:73496968 | T | C | 13 | a0001c0001t0005g0018 a0001c0001t0005g0020 a0001c0001t0005g0021 others(10): Show |
16 | HG01496.hp1 HG01978.hp1 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.1757-768T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496968 | |||||||
chr6:73497002 | C | T | 3 | a0001c0001t0034g0138 a0001c0001t0034g0149 a0001c0001t0065g0152 |
3 | HG00280.hp1 HG01358.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1757-734C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497002 | |||||||
chr6:73497084 | CAT | C | 3 | a0001c0001t0097g0143 a0001c0001t0099g0137 a0001c0001t0100g0153 |
3 | HG02717.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1757-650_1757-649d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497084 | ||||||
chr6:73497157 | C | CTTTTTTT others(3): Show |
39 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0001g0245 others(36): Show |
44 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1757-575_1757-566d others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | ||||||
chr6:73497157 | C | CTTTTTTT others(4): Show |
204 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0130 others(201): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1757-576_1757-566d others(13): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | ||||||
chr6:73497157 | C | CTTTTTTT others(5): Show |
69 | a0001c0001t0001g0131 a0001c0001t0001g0178 a0001c0001t0001g0246 others(66): Show |
69 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1757-577_1757-566d others(14): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | ||||||
chr6:73497157 | C | CTTTTTTT others(6): Show |
21 | a0001c0001t0004g0293 a0001c0001t0016g0185 a0001c0002t0002g0025 others(18): Show |
21 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1757-578_1757-566d others(15): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | ||||||
chr6:73497157 | C | CTTTTTTT others(7): Show |
2 | a0001c0002t0011g0068 a0001c0002t0127g0082 |
2 | HG02738.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1757-566_1757-565i others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | ||||||
chr6:73497240 | C | T | 1 | a0001c0002t0002g0057 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1757-496C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497240 | |||||||
chr6:73497373 | C | T | 1 | a0001c0001t0025g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1757-363C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497373 | |||||||
chr6:73497399 | C | T | 3 | a0001c0001t0006g0195 a0001c0001t0006g0255 a0001c0001t0081g0253 |
3 | NA18982.hp2 NA19002.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1757-337C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497399 | |||||||
chr6:73497468 | T | C | 1 | a0001c0001t0008g0338 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1757-268T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497468 | |||||||
chr6:73498107 | G | C | 2 | a0001c0001t0005g0359 a0001c0001t0005g0360 |
2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1917+211G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498107 | |||||||
chr6:73498222 | A | G | 1 | a0001c0001t0007g0212 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1917+326A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498222 | |||||||
chr6:73498315 | G | A | 1 | a0001c0002t0002g0041 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1917+419G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498315 | |||||||
chr6:73498333 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1917+437T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498333 | |||||||
chr6:73498349 | C | G | 1 | a0001c0001t0045g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1917+453C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498349 | |||||||
chr6:73498448 | T | C | 78 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(75): Show |
78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1917+552T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498448 | |||||||
chr6:73498572 | G | C | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1917+676G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498572 | |||||||
chr6:73498744 | G | T | 2 | a0001c0001t0006g0194 a0001c0001t0024g0264 |
2 | HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1917+848G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498744 | |||||||
chr6:73498793 | C | T | 63 | a0001c0001t0057g0295 a0001c0002t0002g0006 a0001c0002t0002g0025 others(60): Show |
63 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1917+897C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498793 | |||||||
chr6:73498873 | T | C | 1 | a0001c0001t0007g0212 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1917+977T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498873 | |||||||
chr6:73498919 | G | A | 1 | a0001c0001t0105g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1917+1023G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498919 | |||||||
chr6:73499006 | C | T | 3 | a0001c0002t0027g0090 a0001c0002t0027g0091 a0001c0002t0027g0092 |
3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1917+1110C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499006 | |||||||
chr6:73499007 | G | A | 1 | a0001c0002t0111g0062 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1917+1111G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499007 | |||||||
chr6:73499066 | C | G | 5 | a0001c0001t0007g0304 a0001c0001t0007g0326 a0001c0001t0060g0173 others(2): Show |
5 | NA18969.hp1 NA19056.hp1 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.1917+1170C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499066 | |||||||
chr6:73499090 | A | C | 1 | a0001c0001t0016g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1917+1194A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499090 | |||||||
chr6:73499276 | G | C | 1 | a0001c0001t0007g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1918-1298G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499276 | |||||||
chr6:73499437 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1918-1137G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499437 | |||||||
chr6:73499521 | C | CAA | 65 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(62): Show |
65 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1918-1040_1918-103 others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 73499521 | ||||||
chr6:73499521 | C | CAAA | 12 | a0001c0002t0002g0038 a0001c0002t0011g0068 a0001c0002t0020g0072 others(9): Show |
12 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1918-1041_1918-103 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 73499521 | ||||||
chr6:73499521 | CA | C | 15 | a0001c0001t0001g0133 a0001c0001t0008g0121 a0001c0001t0016g0093 others(12): Show |
15 | HG02622.hp2 HG02717.hp2 HG02897.hp1 others(12): Show |
intron_variant | MODIFIER | c.1918-1039delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 73499521 | ||||||
chr6:73499536 | G | A | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1918-1038G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499536 | |||||||
chr6:73499586 | C | A | 2 | a0001c0002t0021g0071 a0001c0002t0021g0080 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1918-988C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499586 | |||||||
chr6:73499620 | G | A | 1 | a0001c0001t0070g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1918-954G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499620 | |||||||
chr6:73499740 | T | C | 81 | a0001c0002t0002g0006 a0001c0002t0002g0025 a0001c0002t0002g0026 others(78): Show |
81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1918-834T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499740 | |||||||
chr6:73499827 | T | C | 1 | a0002c0009t0010g0276 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1918-747T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499827 | |||||||
chr6:73499946 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0035g0135 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1918-628C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499946 | |||||||
chr6:73499992 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0035g0135 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1918-582A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499992 | |||||||
chr6:73500044 | G | C | 1 | a0001c0001t0007g0212 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1918-530G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500044 | |||||||
chr6:73500090 | C | G | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1918-484C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500090 | |||||||
chr6:73500202 | A | G | 1 | a0001c0001t0082g0260 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1918-372A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500202 | |||||||
chr6:73500240 | A | G | 1 | a0001c0001t0067g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1918-334A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500240 | |||||||
chr6:73500346 | A | G | 57 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0132 others(54): Show |
59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1918-228A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500346 | |||||||
chr6:73500567 | T | G | 10 | a0001c0002t0020g0072 a0001c0002t0020g0075 a0001c0002t0020g0076 others(7): Show |
10 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1918-7T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500567 |