Item | Value |
---|---|
geneid | 6949 |
ensemblid | ENSG00000070814.22 |
hgncid | 11654 |
symbol | TCOF1 |
name | treacle ribosome biogenesis factor 1 |
refseq_nuc | NM_001371623.1 |
refseq_prot | NP_001358552.1 |
ensembl_nuc | ENST00000643257.2 |
ensembl_prot | ENSP00000493815.1 |
mane_status | MANE Select |
chr | chr5 |
start | 150357697 |
end | 150400293 |
strand | + |
ver | v1.2 |
region | chr5:150357697-150400293 |
region5000 | chr5:150352697-150405293 |
regionname0 | TCOF1_chr5_150357697_150400293 |
regionname5000 | TCOF1_chr5_150352697_150405293 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1489 | 206 | 56 | 32 | 92 | 5 | 20 | 69 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0002 | 0/0 | 1489 | 53 | 5 | 7 | 24 | 3 | 14 | 20 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0003 | 0/0 | 1489 | 26 | 1 | 2 | 15 | 2 | 6 | 8 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0004 | 0/0 | 1489 | 26 | 13 | 4 | 5 | 2 | 2 | 4 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0005 | 0/1 | 1489 | 15 | 0 | 8 | 0 | 3 | 3 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0006 | 0/0 | 1489 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0007 | 0/0 | 1489 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0008 | 0/0 | 1489 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0009 | 0/0 | 1489 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0010 | 0/0 | 1489 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0011 | 0/0 | 1489 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0012 | 0/0 | 1489 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0013 | 0/0 | 1489 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0014 | 0/0 | 1489 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0015 | 0/0 | 1489 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0016 | 0/0 | 1489 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0017 | 0/0 | 1489 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0018 | 0/0 | 1489 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0019 | 0/0 | 1489 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0020 | 0/0 | 1489 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0021 | 0/0 | 1489 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0022 | 0/0 | 1489 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
a0023 | 0/0 | 1489 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | MAEAR others(1484): Show |
chr5 | 150352697 | 150405293 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 4467 | 199 | 54 | 30 | 90 | 4 | 20 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0001c0011 | 0/0 | 4467 | 2 | 0 | 2 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0001c0020 | 0/0 | 4467 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0001c0021 | 0/0 | 4467 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0001c0023 | 0/0 | 4467 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0001c0025 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0001c0033 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0002c0002 | 0/0 | 4467 | 51 | 5 | 7 | 24 | 3 | 12 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0002c0012 | 0/0 | 4467 | 2 | 0 | 0 | 0 | 0 | 2 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0003c0003 | 0/0 | 4467 | 24 | 1 | 2 | 13 | 2 | 6 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0003c0010 | 0/0 | 4467 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0004c0004 | 0/0 | 4467 | 24 | 12 | 3 | 5 | 2 | 2 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0004c0019 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0004c0032 | 0/0 | 4467 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0005c0005 | 0/1 | 4467 | 15 | 0 | 8 | 0 | 3 | 3 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0006c0006 | 0/0 | 4467 | 4 | 4 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0006c0015 | 0/0 | 4467 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0007c0007 | 0/0 | 4467 | 4 | 4 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0008c0008 | 0/0 | 4467 | 4 | 4 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0009c0014 | 0/0 | 4467 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0009c0031 | 0/0 | 4467 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0010c0009 | 0/0 | 4467 | 3 | 0 | 1 | 0 | 1 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0011c0016 | 0/0 | 4467 | 2 | 0 | 0 | 1 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0012c0017 | 0/0 | 4467 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0013c0013 | 0/0 | 4467 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0014c0034 | 0/0 | 4467 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0015c0024 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0016c0027 | 0/0 | 4467 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0017c0035 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0018c0028 | 0/0 | 4467 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0019c0029 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0020c0022 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0021c0026 | 0/0 | 4467 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0022c0018 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 | ||
a0023c0030 | 0/0 | 4467 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | ATGGC others(4462): Show |
chr5 | 150352697 | 150405293 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5026 | 195 | 53 | 29 | 89 | 3 | 20 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0001c0001t0002 | 0/0 | 5027 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5022): Show |
chr5 | 150352697 | 150405293 |
a0001c0001t0005 | 0/0 | 5026 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0001c0001t0008 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0001c0001t0009 | 0/0 | 5026 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0001c0011t0001 | 0/0 | 5026 | 2 | 0 | 2 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0001c0020t0001 | 0/0 | 5026 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0001c0021t0001 | 0/0 | 5026 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0001c0023t0001 | 0/0 | 5026 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0001c0025t0001 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0001c0033t0006 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0002c0002t0001 | 0/0 | 5026 | 50 | 5 | 6 | 24 | 3 | 12 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0002c0002t0010 | 0/0 | 5026 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0002c0012t0001 | 0/0 | 5026 | 2 | 0 | 0 | 0 | 0 | 2 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0003c0003t0001 | 0/0 | 5026 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0003c0003t0002 | 0/0 | 5027 | 23 | 1 | 2 | 12 | 2 | 6 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5022): Show |
chr5 | 150352697 | 150405293 |
a0003c0010t0002 | 0/0 | 5027 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5022): Show |
chr5 | 150352697 | 150405293 |
a0004c0004t0001 | 0/0 | 5026 | 23 | 11 | 3 | 5 | 2 | 2 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0004c0004t0007 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0004c0019t0001 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0004c0032t0001 | 0/0 | 5026 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0005c0005t0001 | 0/1 | 5026 | 12 | 0 | 6 | 0 | 3 | 2 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0005c0005t0003 | 0/0 | 5026 | 3 | 0 | 2 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0006c0006t0001 | 0/0 | 5026 | 3 | 3 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0006c0006t0002 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5022): Show |
chr5 | 150352697 | 150405293 |
a0006c0015t0001 | 0/0 | 5026 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0007c0007t0001 | 0/0 | 5026 | 4 | 4 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0008c0008t0001 | 0/0 | 5026 | 4 | 4 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0009c0014t0001 | 0/0 | 5026 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0009c0031t0001 | 0/0 | 5026 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0010c0009t0001 | 0/0 | 5026 | 3 | 0 | 1 | 0 | 1 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0011c0016t0004 | 0/0 | 5026 | 2 | 0 | 0 | 1 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0012c0017t0001 | 0/0 | 5026 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0013c0013t0001 | 0/0 | 5026 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0014c0034t0001 | 0/0 | 5026 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0015c0024t0001 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0016c0027t0001 | 0/0 | 5026 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0017c0035t0005 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0018c0028t0001 | 0/0 | 5026 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0019c0029t0001 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0020c0022t0001 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0021c0026t0001 | 0/0 | 5026 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0022c0018t0001 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
a0023c0030t0001 | 0/0 | 5026 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | GGGGA others(5021): Show |
chr5 | 150352697 | 150405293 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0002 | 0/0 | 10 | 1 | 0 | 8 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0030 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0001t0009g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0011t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0020t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0021t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0023t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0025t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0001c0033t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0001 | 0/0 | 12 | 0 | 1 | 7 | 1 | 3 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0005 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0002t0010g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0012t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0002c0012t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0007 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0010t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0003c0010t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0004t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0019t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0004c0032t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0005c0005t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0006c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0006c0006t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0006c0006t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0006c0006t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0006c0015t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0006c0015t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0007c0007t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0007c0007t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0007c0007t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0008c0008t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0008c0008t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0008c0008t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0009c0014t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0009c0014t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0009c0031t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0010c0009t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0010c0009t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0011c0016t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0011c0016t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0012c0017t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0012c0017t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0013c0013t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0013c0013t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0014c0034t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0015c0024t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0016c0027t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0017c0035t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0018c0028t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0019c0029t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0020c0022t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0021c0026t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0022c0018t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
a0023c0030t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0005 | t0001 | g0050 | EUR | GBR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00140 | hp1 | a0003 | c0003 | t0002 | g0071 | EUR | GBR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00280 | hp1 | a0001 | c0021 | t0001 | g0193 | EUR | FIN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00323 | hp1 | a0001 | c0001 | t0009 | g0092 | EUR | FIN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00323 | hp2 | a0005 | c0005 | t0001 | g0225 | EUR | FIN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00423 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00609 | hp2 | a0001 | c0020 | t0001 | g0002 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00639 | hp1 | a0001 | c0011 | t0001 | g0009 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00642 | hp2 | a0005 | c0005 | t0001 | g0246 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00673 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00738 | hp2 | a0002 | c0002 | t0010 | g0037 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00741 | hp1 | a0005 | c0005 | t0001 | g0016 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01099 | hp2 | a0004 | c0004 | t0001 | g0024 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01106 | hp2 | a0001 | c0011 | t0001 | g0009 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01167 | hp1 | a0004 | c0004 | t0001 | g0024 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01175 | hp1 | a0005 | c0005 | t0001 | g0242 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01192 | hp1 | a0005 | c0005 | t0001 | g0050 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01243 | hp1 | a0004 | c0032 | t0001 | g0254 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01243 | hp2 | a0009 | c0031 | t0001 | g0248 | AMR | PUR | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01256 | hp2 | a0005 | c0005 | t0003 | g0016 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01257 | hp2 | a0014 | c0034 | t0001 | g0037 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01346 | hp1 | a0005 | c0005 | t0001 | g0241 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01361 | hp1 | a0003 | c0003 | t0002 | g0011 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01361 | hp2 | a0004 | c0004 | t0001 | g0025 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01433 | hp1 | a0003 | c0003 | t0002 | g0011 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01516 | hp1 | a0004 | c0004 | t0001 | g0056 | EUR | IBS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0184 | EUR | IBS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01517 | hp1 | a0004 | c0004 | t0001 | g0055 | EUR | IBS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01517 | hp2 | a0005 | c0005 | t0001 | g0245 | EUR | IBS | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01891 | hp1 | a0004 | c0004 | t0001 | g0108 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01928 | hp1 | a0005 | c0005 | t0003 | g0243 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01934 | hp2 | a0010 | c0009 | t0001 | g0033 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01978 | hp1 | a0005 | c0005 | t0001 | g0239 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02015 | hp1 | a0003 | c0003 | t0002 | g0010 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02055 | hp1 | a0006 | c0015 | t0001 | g0096 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02080 | hp1 | a0004 | c0004 | t0001 | g0076 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02080 | hp2 | a0003 | c0003 | t0002 | g0020 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02132 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02132 | hp2 | a0003 | c0003 | t0002 | g0020 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02135 | hp2 | a0011 | c0016 | t0004 | g0090 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02145 | hp1 | a0008 | c0008 | t0001 | g0045 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02257 | hp1 | a0003 | c0003 | t0002 | g0070 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02258 | hp2 | a0009 | c0014 | t0001 | g0221 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02280 | hp2 | a0004 | c0004 | t0001 | g0022 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02523 | hp1 | a0003 | c0003 | t0002 | g0010 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02572 | hp2 | a0012 | c0017 | t0001 | g0103 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02602 | hp1 | a0003 | c0003 | t0002 | g0007 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02602 | hp2 | a0002 | c0012 | t0001 | g0175 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02615 | hp1 | a0008 | c0008 | t0001 | g0220 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02622 | hp1 | a0004 | c0004 | t0007 | g0149 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0063 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02630 | hp2 | a0008 | c0008 | t0001 | g0045 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02647 | hp1 | a0006 | c0015 | t0001 | g0093 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02647 | hp2 | a0007 | c0007 | t0001 | g0249 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02698 | hp1 | a0005 | c0005 | t0001 | g0216 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02723 | hp1 | a0007 | c0007 | t0001 | g0051 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02738 | hp2 | a0004 | c0004 | t0001 | g0104 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02809 | hp1 | a0006 | c0006 | t0001 | g0189 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02895 | hp1 | a0006 | c0006 | t0001 | g0039 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02897 | hp2 | a0006 | c0006 | t0002 | g0039 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02922 | hp1 | a0015 | c0024 | t0001 | g0172 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02965 | hp2 | a0004 | c0004 | t0001 | g0187 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02976 | hp1 | a0009 | c0014 | t0001 | g0207 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02976 | hp2 | a0004 | c0004 | t0001 | g0025 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03017 | hp2 | a0016 | c0027 | t0001 | g0001 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03041 | hp1 | a0012 | c0017 | t0001 | g0215 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03130 | hp2 | a0017 | c0035 | t0005 | g0223 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03195 | hp1 | a0004 | c0004 | t0001 | g0252 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0017 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03239 | hp1 | a0018 | c0028 | t0001 | g0163 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03453 | hp2 | a0004 | c0004 | t0001 | g0022 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03486 | hp2 | a0020 | c0022 | t0001 | g0196 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03490 | hp1 | a0005 | c0005 | t0003 | g0016 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0058 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03516 | hp1 | a0004 | c0019 | t0001 | g0188 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03579 | hp2 | a0004 | c0004 | t0001 | g0255 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03654 | hp1 | a0005 | c0005 | t0001 | g0244 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0256 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03704 | hp2 | a0021 | c0026 | t0001 | g0236 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03831 | hp1 | a0003 | c0003 | t0002 | g0072 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03834 | hp1 | a0011 | c0016 | t0004 | g0091 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03834 | hp2 | a0003 | c0003 | t0002 | g0066 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03927 | hp1 | a0003 | c0003 | t0002 | g0011 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03927 | hp2 | a0002 | c0012 | t0001 | g0174 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03942 | hp2 | a0003 | c0003 | t0002 | g0067 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0061 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0060 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG04228 | hp2 | a0004 | c0004 | t0001 | g0105 | SAS | STU | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18522 | hp2 | a0007 | c0007 | t0001 | g0051 | AFR | YRI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | YRI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18940 | hp2 | a0003 | c0010 | t0002 | g0068 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18947 | hp1 | a0013 | c0013 | t0001 | g0002 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0069 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18965 | hp2 | a0004 | c0004 | t0001 | g0041 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18981 | hp2 | a0003 | c0003 | t0002 | g0010 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18986 | hp1 | a0004 | c0004 | t0001 | g0205 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18988 | hp2 | a0013 | c0013 | t0001 | g0124 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18991 | hp1 | a0004 | c0004 | t0001 | g0106 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18994 | hp2 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18998 | hp1 | a0003 | c0010 | t0002 | g0062 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19011 | hp1 | a0001 | c0023 | t0001 | g0134 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19012 | hp2 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19030 | hp1 | a0022 | c0018 | t0001 | g0251 | AFR | LWK | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19030 | hp2 | a0004 | c0004 | t0001 | g0107 | AFR | LWK | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19057 | hp2 | a0004 | c0004 | t0001 | g0041 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19076 | hp2 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19086 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19087 | hp2 | a0023 | c0030 | t0001 | g0186 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19240 | hp1 | a0008 | c0008 | t0001 | g0219 | AFR | YRI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA19240 | hp2 | a0001 | c0033 | t0006 | g0238 | AFR | YRI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ASW | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20129 | hp2 | a0004 | c0004 | t0001 | g0017 | AFR | ASW | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20752 | hp1 | a0010 | c0009 | t0001 | g0033 | EUR | TSI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0110 | EUR | TSI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20805 | hp2 | a0003 | c0003 | t0002 | g0007 | EUR | TSI | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20905 | hp1 | a0003 | c0003 | t0002 | g0065 | SAS | GIH | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20905 | hp2 | a0010 | c0009 | t0001 | g0151 | SAS | GIH | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02109 | hp2 | a0007 | c0007 | t0001 | g0250 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03471 | hp1 | a0001 | c0025 | t0001 | g0120 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG03471 | hp2 | a0019 | c0029 | t0001 | g0125 | AFR | MSL | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | USA | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
HG06807 | hp2 | a0004 | c0004 | t0001 | g0017 | AFR | USA | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | USA | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
NA20300 | hp2 | a0006 | c0006 | t0001 | g0202 | AFR | USA | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
homoSapiens | chm13v2 | a0005 | c0005 | t0001 | g0240 | REF | REF | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0030 | REF | REF | TCOF1_chr5_150352697_150405293 | TCOF1 | chr5 | 150352697 | 150405293 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150368840 | C | T | 1 | a0014 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.503C>T | p.Thr168Met | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 5/27 | 553/5026 | 503/4470 | 168/1489 | chr5 | 150368840 | |||
chr5:150374653 | G | T | 1 | a0011 | 2 | HG02135.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.1120G>T | p.Ala374Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 9/27 | 1170/5026 | 1120/4470 | 374/1489 | chr5 | 150374653 | |||
chr5:150374666 | C | T | 1 | a0007 | 4 | HG02109.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
missense_variant | MODERATE | c.1133C>T | p.Ala378Val | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 9/27 | 1183/5026 | 1133/4470 | 378/1489 | chr5 | 150374666 | |||
chr5:150374762 | C | T | 1 | a0006 | 6 | HG02055.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
missense_variant | MODERATE | c.1229C>T | p.Ser410Leu | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 9/27 | 1279/5026 | 1229/4470 | 410/1489 | chr5 | 150374762 | |||
chr5:150374975 | C | T | 1 | a0012 | 2 | HG02572.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.1300C>T | p.Pro434Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 10/27 | 1350/5026 | 1300/4470 | 434/1489 | chr5 | 150374975 | |||
chr5:150376181 | G | C | 1 | a0003 | 26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
missense_variant | MODERATE | c.1993G>C | p.Ala665Pro | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 13/27 | 2043/5026 | 1993/4470 | 665/1489 | chr5 | 150376181 | |||
chr5:150376276 | T | G | 1 | a0020 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.2088T>G | p.Ser696Arg | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 13/27 | 2138/5026 | 2088/4470 | 696/1489 | chr5 | 150376276 | |||
chr5:150376525 | C | T | 2 | a0008 a0017 |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.2245C>T | p.Pro749Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/27 | 2295/5026 | 2245/4470 | 749/1489 | chr5 | 150376525 | |||
chr5:150379325 | C | G | 1 | a0023 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.2575C>G | p.Gln859Glu | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 16/27 | 2625/5026 | 2575/4470 | 859/1489 | chr5 | 150379325 | |||
chr5:150379533 | T | C | 7 | a0003 a0004 a0007 others(4): Show |
64 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(61): Show |
missense_variant&splice_region_variant | MODERATE | c.2660T>C | p.Val887Ala | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/27 | 2710/5026 | 2660/4470 | 887/1489 | chr5 | 150379533 | |||
chr5:150379635 | C | T | 1 | a0022 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2762C>T | p.Pro921Leu | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/27 | 2812/5026 | 2762/4470 | 921/1489 | chr5 | 150379635 | |||
chr5:150379638 | C | T | 2 | a0007 a0009 |
7 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
missense_variant | MODERATE | c.2765C>T | p.Ser922Leu | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/27 | 2815/5026 | 2765/4470 | 922/1489 | chr5 | 150379638 | |||
chr5:150379715 | G | T | 1 | a0013 | 2 | NA18947.hp1 NA18988.hp2 |
missense_variant | MODERATE | c.2842G>T | p.Ala948Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/27 | 2892/5026 | 2842/4470 | 948/1489 | chr5 | 150379715 | |||
chr5:150392014 | G | T | 1 | a0019 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.3355G>T | p.Ala1119Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 21/27 | 3405/5026 | 3355/4470 | 1119/1489 | chr5 | 150392014 | |||
chr5:150392717 | C | G | 2 | a0005 a0018 |
15 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(12): Show |
missense_variant | MODERATE | c.3530C>G | p.Pro1177Arg | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 22/27 | 3580/5026 | 3530/4470 | 1177/1489 | chr5 | 150392717 | |||
chr5:150393480 | G | A | 1 | a0015 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.3712G>A | p.Ala1238Thr | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/27 | 3762/5026 | 3712/4470 | 1238/1489 | chr5 | 150393480 | |||
chr5:150396282 | G | T | 1 | a0017 | 1 | HG03130.hp2 | missense_variant&splice_region_variant | MODERATE | c.3785G>T | p.Gly1262Val | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/27 | 3835/5026 | 3785/4470 | 1262/1489 | chr5 | 150396282 | |||
chr5:150396504 | A | G | 1 | a0016 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.4007A>G | p.Lys1336Arg | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/27 | 4057/5026 | 4007/4470 | 1336/1489 | chr5 | 150396504 | |||
chr5:150396596 | A | C | 1 | a0021 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.4099A>C | p.Lys1367Gln | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/27 | 4149/5026 | 4099/4470 | 1367/1489 | chr5 | 150396596 | |||
chr5:150396669 | C | T | 7 | a0002 a0010 a0014 others(4): Show |
61 | HG00099.hp2 HG00544.hp1 HG00738.hp2 others(58): Show |
missense_variant | MODERATE | c.4172C>T | p.Ala1391Val | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/27 | 4222/5026 | 4172/4470 | 1391/1489 | chr5 | 150396669 | |||
chr5:150396792 | G | C | 1 | a0010 | 3 | HG01934.hp2 NA20752.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.4295G>C | p.Gly1432Ala | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/27 | 4345/5026 | 4295/4470 | 1432/1489 | chr5 | 150396792 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150361209 | A | G | 2 | a0008c0008 a0017c0035 |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.162A>G | p.Gln54Gln | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/27 | 212/5026 | 162/4470 | 54/1489 | chr5 | 150361209 | |||
chr5:150368871 | C | T | 1 | a0012c0017 | 2 | HG02572.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.534C>T | p.Ser178Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 5/27 | 584/5026 | 534/4470 | 178/1489 | chr5 | 150368871 | |||
chr5:150369542 | G | A | 1 | a0022c0018 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.579G>A | p.Ala193Ala | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/27 | 629/5026 | 579/4470 | 193/1489 | chr5 | 150369542 | |||
chr5:150369563 | C | T | 1 | a0001c0033 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.600C>T | p.Ser200Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/27 | 650/5026 | 600/4470 | 200/1489 | chr5 | 150369563 | |||
chr5:150374619 | G | A | 1 | a0004c0019 | 1 | HG03516.hp1 | splice_region_variant&synonymous_variant | LOW | c.1086G>A | p.Ala362Ala | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 9/27 | 1136/5026 | 1086/4470 | 362/1489 | chr5 | 150374619 | |||
chr5:150374802 | G | A | 1 | a0003c0010 | 2 | NA18940.hp2 NA18998.hp1 |
synonymous_variant | LOW | c.1269G>A | p.Ala423Ala | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 9/27 | 1319/5026 | 1269/4470 | 423/1489 | chr5 | 150374802 | |||
chr5:150374956 | G | A | 1 | a0001c0011 | 2 | HG00639.hp1 HG01106.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1281G>A | p.Ala427Ala | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 10/27 | 1331/5026 | 1281/4470 | 427/1489 | chr5 | 150374956 | |||
chr5:150374974 | C | A | 1 | a0001c0020 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.1299C>A | p.Ala433Ala | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 10/27 | 1349/5026 | 1299/4470 | 433/1489 | chr5 | 150374974 | |||
chr5:150375428 | C | T | 10 | a0003c0003 a0003c0010 a0004c0004 others(7): Show |
63 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(60): Show |
synonymous_variant | LOW | c.1578C>T | p.Pro526Pro | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 11/27 | 1628/5026 | 1578/4470 | 526/1489 | chr5 | 150375428 | |||
chr5:150375440 | G | A | 1 | a0002c0012 | 2 | HG02602.hp2 HG03927.hp2 |
synonymous_variant | LOW | c.1590G>A | p.Gly530Gly | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 11/27 | 1640/5026 | 1590/4470 | 530/1489 | chr5 | 150375440 | |||
chr5:150375521 | T | C | 1 | a0001c0021 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.1671T>C | p.Asp557Asp | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 11/27 | 1721/5026 | 1671/4470 | 557/1489 | chr5 | 150375521 | |||
chr5:150375777 | G | T | 5 | a0004c0004 a0004c0019 a0004c0032 others(2): Show |
30 | HG01099.hp2 HG01167.hp1 HG01243.hp1 others(27): Show |
synonymous_variant | LOW | c.1761G>T | p.Gly587Gly | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 12/27 | 1811/5026 | 1761/4470 | 587/1489 | chr5 | 150375777 | |||
chr5:150375858 | A | G | 11 | a0003c0003 a0003c0010 a0004c0004 others(8): Show |
64 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(61): Show |
synonymous_variant | LOW | c.1842A>G | p.Ser614Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 12/27 | 1892/5026 | 1842/4470 | 614/1489 | chr5 | 150375858 | |||
chr5:150376282 | A | G | 3 | a0007c0007 a0009c0014 a0009c0031 |
7 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
synonymous_variant | LOW | c.2094A>G | p.Glu698Glu | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 13/27 | 2144/5026 | 2094/4470 | 698/1489 | chr5 | 150376282 | |||
chr5:150379273 | G | A | 1 | a0001c0023 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.2523G>A | p.Ala841Ala | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 16/27 | 2573/5026 | 2523/4470 | 841/1489 | chr5 | 150379273 | |||
chr5:150392085 | C | T | 1 | a0012c0017 | 2 | HG02572.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.3426C>T | p.Ser1142Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 21/27 | 3476/5026 | 3426/4470 | 1142/1489 | chr5 | 150392085 | |||
chr5:150392169 | C | T | 1 | a0006c0006 | 4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.3510C>T | p.His1170His | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 21/27 | 3560/5026 | 3510/4470 | 1170/1489 | chr5 | 150392169 | |||
chr5:150392781 | G | A | 1 | a0009c0031 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.3594G>A | p.Ala1198Ala | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 22/27 | 3644/5026 | 3594/4470 | 1198/1489 | chr5 | 150392781 | |||
chr5:150396550 | G | A | 2 | a0009c0014 a0009c0031 |
3 | HG01243.hp2 HG02258.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.4053G>A | p.Ser1351Ser | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/27 | 4103/5026 | 4053/4470 | 1351/1489 | chr5 | 150396550 | |||
chr5:150399036 | G | A | 2 | a0001c0025 a0004c0032 |
2 | HG01243.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.4458G>A | p.Glu1486Glu | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/27 | 4508/5026 | 4458/4470 | 1486/1489 | chr5 | 150399036 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150399049 | C | T | 2 | a0001c0001t0005 a0017c0035t0005 |
2 | HG01952.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/27 | 1 | chr5 | 150399049 | ||||||
chr5:150399845 | T | G | 1 | a0001c0033t0006 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*58T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 27/27 | 797 | chr5 | 150399845 | ||||||
chr5:150399858 | G | A | 1 | a0011c0016t0004 | 2 | HG02135.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*71G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 27/27 | 810 | chr5 | 150399858 | ||||||
chr5:150399928 | T | G | 1 | a0004c0004t0007 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*141T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 27/27 | 880 | chr5 | 150399928 | ||||||
chr5:150400028 | A | G | 1 | a0004c0004t0007 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 27/27 | 980 | chr5 | 150400028 | ||||||
chr5:150400147 | G | C | 1 | a0001c0001t0008 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 27/27 | 1099 | chr5 | 150400147 | ||||||
chr5:150400173 | G | A | 1 | a0001c0001t0009 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*386G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 27/27 | 1125 | chr5 | 150400173 | ||||||
chr5:150400177 | C | T | 1 | a0005c0005t0003 | 3 | HG01256.hp2 HG01928.hp1 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*390C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 27/27 | 1129 | chr5 | 150400177 | ||||||
chr5:150400217 | C | T | 1 | a0002c0002t0010 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*430C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 27/27 | 1169 | chr5 | 150400217 | ||||||
chr5:150400243 | G | GT | 4 | a0001c0001t0002 a0003c0003t0002 a0003c0010t0002 others(1): Show |
27 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*466dupT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 27/27 | 1206 | INFO_REALIGN_3_PRIME | chr5 | 150400243 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150357905 | AGCGGCCC | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | NA18983.hp1 NA18989.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.108+62_108+68delGC others(5): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr5 | 150357905 | ||||||
chr5:150358165 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.108+311C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358165 | |||||||
chr5:150358199 | G | A | 2 | a0004c0004t0001g0055 a0004c0004t0001g0056 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.108+345G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358199 | |||||||
chr5:150358260 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.108+406G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358260 | |||||||
chr5:150358353 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.108+499A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358353 | |||||||
chr5:150358391 | T | C | 4 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(1): Show |
4 | HG03491.hp2 HG03669.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+537T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358391 | |||||||
chr5:150358396 | C | T | 1 | a0002c0002t0001g0256 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.108+542C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358396 | |||||||
chr5:150358446 | A | G | 6 | a0001c0001t0001g0253 a0004c0004t0001g0017 a0004c0004t0001g0252 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.108+592A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358446 | |||||||
chr5:150358705 | C | T | 4 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(1): Show |
5 | HG01243.hp2 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.108+851C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358705 | |||||||
chr5:150358772 | G | A | 1 | a0003c0010t0002g0062 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.108+918G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358772 | |||||||
chr5:150358972 | T | C | 1 | a0001c0001t0008g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.108+1118T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150358972 | |||||||
chr5:150359045 | T | A | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.108+1191T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150359045 | |||||||
chr5:150359192 | C | T | 1 | a0002c0002t0001g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.108+1338C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150359192 | |||||||
chr5:150359197 | A | T | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.108+1343A>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150359197 | |||||||
chr5:150359331 | G | A | 6 | a0001c0001t0001g0253 a0004c0004t0001g0017 a0004c0004t0001g0252 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.108+1477G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150359331 | |||||||
chr5:150359346 | C | CA | 21 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0073 others(18): Show |
21 | HG00280.hp2 HG00597.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.108+1506dupA | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr5 | 150359346 | ||||||
chr5:150359556 | C | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0048 others(38): Show |
48 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.109-1600C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150359556 | |||||||
chr5:150359872 | C | T | 1 | a0017c0035t0005g0223 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.109-1284C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150359872 | |||||||
chr5:150359981 | C | G | 4 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(1): Show |
5 | HG01243.hp2 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-1175C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150359981 | |||||||
chr5:150360005 | G | A | 1 | a0003c0003t0002g0065 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.109-1151G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360005 | |||||||
chr5:150360226 | A | G | 3 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 |
4 | HG02109.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-930A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360226 | |||||||
chr5:150360315 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0083 |
6 | HG00140.hp2 HG00280.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-841C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360315 | |||||||
chr5:150360487 | C | A | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.109-669C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360487 | |||||||
chr5:150360510 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.109-646G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360510 | |||||||
chr5:150360675 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.109-481G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360675 | |||||||
chr5:150360677 | T | A | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.109-479T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360677 | |||||||
chr5:150360732 | C | CT | 42 | a0001c0001t0001g0052 a0001c0001t0001g0073 a0001c0001t0001g0217 others(39): Show |
56 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.109-403dupT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr5 | 150360732 | ||||||
chr5:150360732 | CT | C | 13 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0097 others(10): Show |
14 | HG00323.hp1 HG01517.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.109-403delT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr5 | 150360732 | ||||||
chr5:150360791 | C | T | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.109-365C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360791 | |||||||
chr5:150360868 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.109-288C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360868 | |||||||
chr5:150360869 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0098 others(6): Show |
15 | HG01192.hp2 HG01433.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.109-287C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150360869 | |||||||
chr5:150361128 | T | C | 1 | a0022c0018t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.109-28T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150361128 | |||||||
chr5:150361143 | T | C | 3 | a0001c0001t0001g0100 a0002c0002t0001g0023 a0002c0002t0001g0214 |
4 | HG01496.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-13T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 1/26 | chr5 | 150361143 | |||||||
chr5:150361308 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.164+97C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150361308 | |||||||
chr5:150361310 | A | G | 2 | a0009c0014t0001g0207 a0009c0014t0001g0221 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.164+99A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150361310 | |||||||
chr5:150361417 | G | A | 1 | a0017c0035t0005g0223 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.164+206G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150361417 | |||||||
chr5:150361833 | G | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.164+622G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150361833 | |||||||
chr5:150361924 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.164+713C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150361924 | |||||||
chr5:150362008 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0082 |
5 | HG02083.hp2 HG02155.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+797C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150362008 | |||||||
chr5:150362051 | G | A | 1 | a0005c0005t0001g0239 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.164+840G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150362051 | |||||||
chr5:150362119 | T | C | 3 | a0004c0004t0001g0022 a0011c0016t0004g0090 a0011c0016t0004g0091 |
4 | HG02135.hp2 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+908T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150362119 | |||||||
chr5:150362342 | C | G | 3 | a0001c0001t0001g0204 a0004c0004t0001g0041 a0004c0004t0001g0205 |
4 | NA18965.hp2 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+1131C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150362342 | |||||||
chr5:150362368 | A | G | 6 | a0001c0001t0001g0253 a0004c0004t0001g0017 a0004c0004t0001g0252 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.164+1157A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150362368 | |||||||
chr5:150362429 | C | A | 6 | a0001c0001t0001g0253 a0004c0004t0001g0017 a0004c0004t0001g0252 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.164+1218C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150362429 | |||||||
chr5:150362610 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.164+1399C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150362610 | |||||||
chr5:150362673 | G | T | 11 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0231 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.165-1440G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150362673 | |||||||
chr5:150362869 | T | C | 5 | a0004c0004t0001g0022 a0011c0016t0004g0090 a0011c0016t0004g0091 others(2): Show |
6 | HG02135.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.165-1244T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150362869 | |||||||
chr5:150363147 | T | G | 1 | a0002c0002t0001g0075 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.165-966T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363147 | |||||||
chr5:150363181 | C | T | 1 | a0006c0006t0001g0202 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165-932C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363181 | |||||||
chr5:150363262 | T | G | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.165-851T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363262 | |||||||
chr5:150363314 | T | G | 24 | a0001c0001t0001g0204 a0001c0001t0001g0253 a0004c0004t0001g0017 others(21): Show |
30 | HG01099.hp2 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.165-799T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363314 | |||||||
chr5:150363359 | G | T | 1 | a0001c0001t0001g0013 | 3 | HG02109.hp1 HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.165-754G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363359 | |||||||
chr5:150363541 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.165-572G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363541 | |||||||
chr5:150363684 | A | G | 4 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 others(1): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-429A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363684 | |||||||
chr5:150363726 | C | T | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.165-387C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363726 | |||||||
chr5:150363844 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0200 a0001c0001t0001g0201 |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-269C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363844 | |||||||
chr5:150363905 | A | T | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.165-208A>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363905 | |||||||
chr5:150363923 | G | T | 4 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 others(1): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-190G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363923 | |||||||
chr5:150363998 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0009g0092 |
6 | HG00323.hp1 HG00423.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-115G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150363998 | |||||||
chr5:150364026 | G | C | 1 | a0002c0002t0001g0110 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.165-87G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150364026 | |||||||
chr5:150364027 | G | T | 1 | a0002c0002t0001g0110 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.165-86G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150364027 | |||||||
chr5:150364045 | T | C | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG01167.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.165-68T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 2/26 | chr5 | 150364045 | |||||||
chr5:150364413 | C | T | 44 | a0001c0001t0001g0204 a0001c0001t0001g0253 a0003c0003t0001g0069 others(41): Show |
61 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.304+161C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150364413 | |||||||
chr5:150364414 | G | A | 1 | a0006c0015t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.304+162G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150364414 | |||||||
chr5:150364426 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.304+174A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150364426 | |||||||
chr5:150364454 | C | T | 13 | a0001c0001t0001g0204 a0004c0004t0001g0024 a0004c0004t0001g0025 others(10): Show |
16 | HG01099.hp2 HG01167.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.304+202C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150364454 | |||||||
chr5:150364663 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(156): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.304+411A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150364663 | |||||||
chr5:150364744 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.304+492C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150364744 | |||||||
chr5:150364814 | A | G | 1 | a0004c0004t0001g0022 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.304+562A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150364814 | |||||||
chr5:150364980 | G | C | 1 | a0001c0001t0008g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.304+728G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150364980 | |||||||
chr5:150365005 | C | A | 1 | a0004c0004t0001g0022 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.304+753C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150365005 | |||||||
chr5:150365115 | C | T | 24 | a0001c0001t0001g0204 a0001c0001t0001g0253 a0004c0004t0001g0017 others(21): Show |
30 | HG01099.hp2 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.304+863C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150365115 | |||||||
chr5:150365222 | T | C | 6 | a0001c0001t0001g0253 a0004c0004t0001g0017 a0004c0004t0001g0252 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.304+970T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150365222 | |||||||
chr5:150365253 | C | CT | 11 | a0001c0001t0001g0073 a0001c0001t0001g0098 a0002c0002t0001g0005 others(8): Show |
12 | HG01167.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.304+1021dupT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150365253 | ||||||
chr5:150365253 | C | CTT | 12 | a0001c0001t0001g0204 a0004c0004t0001g0024 a0004c0004t0001g0025 others(9): Show |
13 | HG01099.hp2 HG01361.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.304+1020_304+1021d others(4): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150365253 | ||||||
chr5:150365253 | CT | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0043 others(9): Show |
14 | HG00323.hp1 HG01167.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.304+1021delT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150365253 | ||||||
chr5:150365253 | CTTTTT | C | 6 | a0001c0001t0001g0253 a0004c0004t0001g0017 a0004c0004t0001g0252 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.304+1017_304+1021d others(7): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150365253 | ||||||
chr5:150365253 | CTTTTTTT others(4): Show |
C | 3 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 |
4 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+1011_304+1021d others(13): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150365253 | ||||||
chr5:150365257 | T | C | 13 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0208 others(10): Show |
19 | HG00423.hp1 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.304+1005T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150365257 | |||||||
chr5:150365258 | T | C | 1 | a0003c0003t0001g0069 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.304+1006T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150365258 | |||||||
chr5:150365845 | G | A | 3 | a0001c0001t0001g0100 a0002c0002t0001g0023 a0002c0002t0001g0214 |
4 | HG01496.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+1593G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150365845 | |||||||
chr5:150365951 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.304+1699T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150365951 | |||||||
chr5:150365989 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.304+1737C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150365989 | |||||||
chr5:150366061 | A | G | 6 | a0001c0001t0001g0253 a0004c0004t0001g0017 a0004c0004t0001g0252 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.305-1783A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150366061 | |||||||
chr5:150366117 | C | CA | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0026 others(21): Show |
35 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.305-1711dupA | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150366117 | ||||||
chr5:150366117 | CA | C | 9 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0253 others(6): Show |
11 | HG01243.hp1 HG01256.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.305-1711delA | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150366117 | ||||||
chr5:150366222 | G | A | 12 | a0005c0005t0001g0016 a0005c0005t0001g0050 a0005c0005t0001g0216 others(9): Show |
14 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.305-1622G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150366222 | |||||||
chr5:150366268 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.305-1576G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150366268 | |||||||
chr5:150366341 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.305-1503A>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150366341 | |||||||
chr5:150366345 | T | A | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.305-1499T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150366345 | |||||||
chr5:150366554 | A | G | 13 | a0001c0001t0001g0204 a0004c0004t0001g0024 a0004c0004t0001g0025 others(10): Show |
16 | HG01099.hp2 HG01167.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.305-1290A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150366554 | |||||||
chr5:150366561 | A | G | 4 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(1): Show |
5 | HG01243.hp2 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-1283A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150366561 | |||||||
chr5:150366628 | GCAACATT others(319): Show |
G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.305-1202_305-877de others(1): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150366628 | ||||||
chr5:150366639 | C | CT | 8 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0052 others(5): Show |
9 | HG02071.hp2 HG04228.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.305-1179dupT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150366639 | ||||||
chr5:150366639 | CT | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0083 others(7): Show |
10 | HG00280.hp2 HG01993.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.305-1179delT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150366639 | ||||||
chr5:150366811 | C | T | 1 | a0001c0011t0001g0009 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.305-1033C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150366811 | |||||||
chr5:150366815 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.305-1029C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150366815 | |||||||
chr5:150366937 | AG | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(94): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.305-905delG | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr5 | 150366937 | ||||||
chr5:150367088 | G | A | 1 | a0003c0003t0002g0070 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.305-756G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367088 | |||||||
chr5:150367149 | C | T | 2 | a0001c0001t0001g0195 a0020c0022t0001g0196 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.305-695C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367149 | |||||||
chr5:150367236 | C | T | 4 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(1): Show |
5 | HG01243.hp2 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-608C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367236 | |||||||
chr5:150367331 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0116 a0001c0001t0001g0217 |
4 | HG02886.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.305-513G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367331 | |||||||
chr5:150367463 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.305-381C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367463 | |||||||
chr5:150367553 | C | T | 2 | a0009c0014t0001g0207 a0009c0014t0001g0221 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.305-291C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367553 | |||||||
chr5:150367588 | G | A | 1 | a0009c0014t0001g0207 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.305-256G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367588 | |||||||
chr5:150367590 | T | C | 2 | a0010c0009t0001g0033 a0010c0009t0001g0151 |
3 | HG01934.hp2 NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.305-254T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367590 | |||||||
chr5:150367722 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.305-122A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367722 | |||||||
chr5:150367792 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.305-52A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367792 | |||||||
chr5:150367808 | C | A | 1 | a0001c0001t0001g0029 | 2 | HG01981.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.305-36C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 3/26 | chr5 | 150367808 | |||||||
chr5:150367933 | T | C | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.378+16T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150367933 | |||||||
chr5:150367956 | T | G | 1 | a0004c0004t0001g0022 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.378+39T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150367956 | |||||||
chr5:150367990 | A | C | 3 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 |
4 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+73A>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150367990 | |||||||
chr5:150367991 | G | T | 3 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 |
4 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+74G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150367991 | |||||||
chr5:150368165 | G | A | 4 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(1): Show |
5 | HG01243.hp2 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+248G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150368165 | |||||||
chr5:150368342 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.379-374A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150368342 | |||||||
chr5:150368403 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.379-313C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150368403 | |||||||
chr5:150368452 | T | C | 1 | a0003c0003t0002g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.379-264T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150368452 | |||||||
chr5:150368509 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.379-207A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150368509 | |||||||
chr5:150368537 | T | G | 3 | a0004c0004t0001g0022 a0011c0016t0004g0090 a0011c0016t0004g0091 |
4 | HG02135.hp2 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-179T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 4/26 | chr5 | 150368537 | |||||||
chr5:150369194 | A | G | 1 | a0004c0004t0001g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.565+292A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 5/26 | chr5 | 150369194 | |||||||
chr5:150369382 | C | T | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.566-147C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 5/26 | chr5 | 150369382 | |||||||
chr5:150369399 | T | C | 4 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 others(1): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-130T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 5/26 | chr5 | 150369399 | |||||||
chr5:150369634 | C | T | 1 | a0001c0021t0001g0193 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.639+32C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150369634 | |||||||
chr5:150369743 | C | T | 1 | a0001c0033t0006g0238 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.639+141C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150369743 | |||||||
chr5:150369846 | C | T | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.639+244C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150369846 | |||||||
chr5:150369904 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.639+302G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150369904 | |||||||
chr5:150369929 | C | T | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.639+327C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150369929 | |||||||
chr5:150369970 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0191 a0001c0001t0001g0192 |
5 | HG01884.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+368A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150369970 | |||||||
chr5:150370242 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.639+640A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150370242 | |||||||
chr5:150370285 | G | A | 1 | a0001c0025t0001g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.639+683G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150370285 | |||||||
chr5:150370403 | T | A | 23 | a0001c0001t0001g0204 a0001c0001t0001g0253 a0004c0004t0001g0017 others(20): Show |
29 | HG01099.hp2 HG01167.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.639+801T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150370403 | |||||||
chr5:150370454 | C | G | 1 | a0007c0007t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.639+852C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150370454 | |||||||
chr5:150370491 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.639+889G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150370491 | |||||||
chr5:150370511 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.639+909A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150370511 | |||||||
chr5:150370655 | C | G | 2 | a0004c0004t0001g0255 a0004c0032t0001g0254 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.639+1053C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150370655 | |||||||
chr5:150371249 | C | T | 1 | a0005c0005t0001g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.640-757C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150371249 | |||||||
chr5:150371345 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
36 | HG00597.hp2 HG00621.hp1 HG02015.hp2 others(33): Show |
intron_variant | MODIFIER | c.640-661G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150371345 | |||||||
chr5:150371358 | G | A | 1 | a0022c0018t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640-648G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150371358 | |||||||
chr5:150371499 | G | A | 2 | a0009c0014t0001g0207 a0009c0014t0001g0221 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.640-507G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150371499 | |||||||
chr5:150371649 | T | G | 1 | a0002c0002t0001g0162 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.640-357T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150371649 | |||||||
chr5:150371783 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
139 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.640-223G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150371783 | |||||||
chr5:150371872 | G | C | 1 | a0018c0028t0001g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.640-134G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 6/26 | chr5 | 150371872 | |||||||
chr5:150372304 | A | G | 2 | a0011c0016t0004g0090 a0011c0016t0004g0091 |
2 | HG02135.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.870+68A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150372304 | |||||||
chr5:150372418 | A | G | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.870+182A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150372418 | |||||||
chr5:150372724 | TG | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(88): Show |
127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.870+492delG | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr5 | 150372724 | ||||||
chr5:150373212 | T | TTG | 3 | a0001c0001t0001g0081 a0001c0001t0001g0237 a0005c0005t0001g0246 |
3 | HG00642.hp1 HG00642.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.871-940_871-939dup others(2): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr5 | 150373212 | ||||||
chr5:150373212 | TTG | T | 7 | a0004c0004t0001g0022 a0007c0007t0001g0051 a0007c0007t0001g0249 others(4): Show |
9 | HG01243.hp2 HG02109.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-940_871-939del others(2): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr5 | 150373212 | ||||||
chr5:150373309 | G | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0197 a0001c0001t0001g0232 others(2): Show |
6 | HG00597.hp1 HG01496.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-865G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373309 | |||||||
chr5:150373420 | T | C | 3 | a0001c0001t0001g0100 a0002c0002t0001g0023 a0002c0002t0001g0214 |
4 | HG01496.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-754T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373420 | |||||||
chr5:150373467 | C | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02015.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.871-707C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373467 | |||||||
chr5:150373472 | C | T | 18 | a0001c0001t0001g0204 a0001c0001t0001g0253 a0004c0004t0001g0017 others(15): Show |
23 | HG01099.hp2 HG01167.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.871-702C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373472 | |||||||
chr5:150373566 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.871-608G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373566 | |||||||
chr5:150373577 | C | T | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.871-597C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373577 | |||||||
chr5:150373581 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0257 |
3 | HG00639.hp2 HG01175.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.871-593G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373581 | |||||||
chr5:150373620 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.871-554C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373620 | |||||||
chr5:150373781 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.871-393G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373781 | |||||||
chr5:150373789 | C | A | 1 | a0001c0025t0001g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.871-385C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373789 | |||||||
chr5:150373864 | G | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | NA18983.hp1 NA18989.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.871-310G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373864 | |||||||
chr5:150373963 | A | G | 1 | a0002c0002t0001g0060 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.871-211A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150373963 | |||||||
chr5:150374084 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.871-90G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 7/26 | chr5 | 150374084 | |||||||
chr5:150374409 | C | G | 1 | a0004c0004t0001g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1083+23C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 8/26 | chr5 | 150374409 | |||||||
chr5:150374425 | G | A | 6 | a0003c0003t0002g0007 a0003c0003t0002g0011 a0003c0003t0002g0066 others(3): Show |
11 | HG00140.hp1 HG00673.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1083+39G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 8/26 | chr5 | 150374425 | |||||||
chr5:150374825 | G | A | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1278+14G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 9/26 | chr5 | 150374825 | |||||||
chr5:150374871 | G | C | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG01167.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1278+60G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 9/26 | chr5 | 150374871 | |||||||
chr5:150374900 | T | C | 1 | a0002c0002t0001g0166 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1279-54T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 9/26 | chr5 | 150374900 | |||||||
chr5:150375179 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1488+16G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 10/26 | chr5 | 150375179 | |||||||
chr5:150375257 | G | A | 11 | a0001c0001t0001g0048 a0001c0001t0001g0232 a0001c0001t0001g0233 others(8): Show |
13 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1489-82G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 10/26 | chr5 | 150375257 | |||||||
chr5:150375570 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1704+16G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 11/26 | chr5 | 150375570 | |||||||
chr5:150375631 | C | T | 1 | a0022c0018t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1704+77C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 11/26 | chr5 | 150375631 | |||||||
chr5:150376393 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2143-30G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 13/26 | chr5 | 150376393 | |||||||
chr5:150376816 | C | T | 1 | a0004c0004t0001g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2340+196C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150376816 | |||||||
chr5:150376906 | G | T | 1 | a0005c0005t0001g0245 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2340+286G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150376906 | |||||||
chr5:150376914 | G | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.2340+294G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150376914 | |||||||
chr5:150377030 | A | G | 1 | a0001c0023t0001g0134 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2340+410A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150377030 | |||||||
chr5:150377199 | G | A | 1 | a0010c0009t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2340+579G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150377199 | |||||||
chr5:150377207 | G | C | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2340+587G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150377207 | |||||||
chr5:150377262 | A | C | 19 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(16): Show |
29 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2340+642A>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150377262 | |||||||
chr5:150377308 | C | T | 1 | a0008c0008t0001g0045 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2340+688C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150377308 | |||||||
chr5:150377406 | T | C | 1 | a0008c0008t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2340+786T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150377406 | |||||||
chr5:150377464 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2340+844G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150377464 | |||||||
chr5:150378185 | T | C | 1 | a0022c0018t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2341-720T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150378185 | |||||||
chr5:150378406 | C | T | 4 | a0004c0004t0001g0041 a0004c0004t0001g0076 a0004c0004t0001g0106 others(1): Show |
5 | HG02080.hp1 NA18965.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.2341-499C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150378406 | |||||||
chr5:150378761 | C | T | 1 | a0006c0015t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2341-144C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150378761 | |||||||
chr5:150378784 | C | T | 1 | a0002c0002t0001g0190 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2341-121C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150378784 | |||||||
chr5:150378817 | C | T | 1 | a0005c0005t0001g0216 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2341-88C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 14/26 | chr5 | 150378817 | |||||||
chr5:150379111 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2478+69C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 15/26 | chr5 | 150379111 | |||||||
chr5:150379502 | TCTCTC | T | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2659-24_2659-20del others(5): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr5 | 150379502 | ||||||
chr5:150379781 | G | A | 5 | a0004c0004t0001g0017 a0004c0004t0001g0252 a0004c0004t0001g0255 others(2): Show |
7 | HG01243.hp1 HG03195.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2859+49G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150379781 | |||||||
chr5:150379901 | G | A | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2859+169G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150379901 | |||||||
chr5:150380070 | C | CA | 10 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0081 others(7): Show |
13 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2859+353dupA | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr5 | 150380070 | ||||||
chr5:150380225 | T | C | 2 | a0002c0002t0001g0075 a0002c0002t0001g0198 |
2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2859+493T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150380225 | |||||||
chr5:150380337 | A | G | 1 | a0004c0004t0007g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2859+605A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150380337 | |||||||
chr5:150380397 | C | T | 4 | a0006c0006t0001g0039 a0006c0006t0001g0189 a0006c0006t0001g0202 others(1): Show |
4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2859+665C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150380397 | |||||||
chr5:150380654 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2859+922A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150380654 | |||||||
chr5:150380784 | G | A | 1 | a0004c0004t0001g0022 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2859+1052G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150380784 | |||||||
chr5:150380936 | G | A | 19 | a0004c0004t0001g0017 a0004c0004t0001g0024 a0004c0004t0001g0025 others(16): Show |
24 | HG01099.hp2 HG01167.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2859+1204G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150380936 | |||||||
chr5:150380967 | C | A | 6 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(3): Show |
7 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2859+1235C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150380967 | |||||||
chr5:150381169 | C | A | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2859+1437C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150381169 | |||||||
chr5:150381260 | T | C | 47 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(44): Show |
64 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.2859+1528T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150381260 | |||||||
chr5:150381369 | C | T | 1 | a0023c0030t0001g0186 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2859+1637C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150381369 | |||||||
chr5:150381373 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2859+1641A>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150381373 | |||||||
chr5:150381391 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0209 a0001c0001t0001g0210 |
8 | HG01192.hp2 HG01928.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.2859+1659G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150381391 | |||||||
chr5:150381620 | A | G | 1 | a0004c0004t0007g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2859+1888A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150381620 | |||||||
chr5:150381673 | T | G | 17 | a0001c0021t0001g0193 a0003c0003t0001g0069 a0003c0003t0002g0007 others(14): Show |
27 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.2859+1941T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150381673 | |||||||
chr5:150381758 | T | C | 1 | a0001c0001t0009g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2859+2026T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150381758 | |||||||
chr5:150382164 | CA | C | 19 | a0004c0004t0001g0017 a0004c0004t0001g0024 a0004c0004t0001g0025 others(16): Show |
24 | HG01099.hp2 HG01167.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2859+2442delA | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr5 | 150382164 | ||||||
chr5:150382182 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2859+2450G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150382182 | |||||||
chr5:150382228 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2859+2496G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150382228 | |||||||
chr5:150382355 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2859+2623C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150382355 | |||||||
chr5:150382362 | G | GT | 13 | a0001c0001t0001g0102 a0001c0001t0001g0231 a0005c0005t0001g0016 others(10): Show |
15 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.2859+2632dupT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr5 | 150382362 | ||||||
chr5:150382403 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2859+2671T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150382403 | |||||||
chr5:150382418 | A | G | 3 | a0004c0004t0001g0017 a0004c0004t0001g0252 a0004c0019t0001g0188 |
5 | HG03195.hp1 HG03209.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2859+2686A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150382418 | |||||||
chr5:150382892 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2859+3160T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150382892 | |||||||
chr5:150383035 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2859+3303G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150383035 | |||||||
chr5:150383176 | C | T | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2859+3444C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150383176 | |||||||
chr5:150383256 | A | C | 6 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(3): Show |
7 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2859+3524A>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150383256 | |||||||
chr5:150383435 | G | A | 6 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(3): Show |
7 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2859+3703G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150383435 | |||||||
chr5:150383449 | C | G | 1 | a0002c0002t0001g0185 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2859+3717C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150383449 | |||||||
chr5:150383699 | G | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
6 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2859+3967G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150383699 | |||||||
chr5:150383742 | A | G | 46 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(43): Show |
63 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.2859+4010A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150383742 | |||||||
chr5:150384209 | T | G | 3 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 |
4 | HG02109.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860-3693T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150384209 | |||||||
chr5:150384259 | G | T | 3 | a0004c0004t0001g0022 a0011c0016t0004g0090 a0011c0016t0004g0091 |
4 | HG02135.hp2 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860-3643G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150384259 | |||||||
chr5:150384321 | C | G | 1 | a0011c0016t0004g0090 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2860-3581C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150384321 | |||||||
chr5:150384556 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2860-3346C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150384556 | |||||||
chr5:150384563 | G | A | 2 | a0003c0003t0002g0018 a0003c0003t0002g0064 |
3 | NA18994.hp2 NA19012.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2860-3339G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150384563 | |||||||
chr5:150384609 | A | G | 1 | a0009c0031t0001g0248 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2860-3293A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150384609 | |||||||
chr5:150384625 | C | G | 1 | a0002c0002t0001g0184 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2860-3277C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150384625 | |||||||
chr5:150384675 | G | GTC | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(158): Show |
219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.2860-3225_2860-322 others(6): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr5 | 150384675 | ||||||
chr5:150384730 | T | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
144 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.2860-3172T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150384730 | |||||||
chr5:150384732 | G | A | 1 | a0001c0020t0001g0002 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2860-3170G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150384732 | |||||||
chr5:150385080 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2860-2822G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385080 | |||||||
chr5:150385085 | A | C | 1 | a0001c0001t0008g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2860-2817A>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385085 | |||||||
chr5:150385259 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2860-2643A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385259 | |||||||
chr5:150385314 | T | C | 1 | a0001c0001t0001g0013 | 3 | HG02109.hp1 HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2860-2588T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385314 | |||||||
chr5:150385319 | G | C | 1 | a0002c0002t0001g0169 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2860-2583G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385319 | |||||||
chr5:150385330 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2860-2572C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385330 | |||||||
chr5:150385474 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2860-2428C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385474 | |||||||
chr5:150385542 | A | G | 3 | a0005c0005t0001g0216 a0005c0005t0001g0244 a0005c0005t0001g0246 |
3 | HG00642.hp2 HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2860-2360A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385542 | |||||||
chr5:150385777 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(100): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.2860-2125A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385777 | |||||||
chr5:150385781 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2860-2121T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385781 | |||||||
chr5:150385864 | C | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0034 others(28): Show |
44 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.2860-2038C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385864 | |||||||
chr5:150385870 | G | GT | 4 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 others(1): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860-2024dupT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr5 | 150385870 | ||||||
chr5:150385871 | T | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0081 a0001c0001t0001g0191 others(1): Show |
6 | HG01884.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2860-2031T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150385871 | |||||||
chr5:150386089 | G | A | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2860-1813G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150386089 | |||||||
chr5:150386181 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
138 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.2860-1721C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150386181 | |||||||
chr5:150386351 | C | A | 2 | a0003c0003t0002g0018 a0003c0003t0002g0064 |
3 | NA18994.hp2 NA19012.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2860-1551C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150386351 | |||||||
chr5:150386422 | T | C | 2 | a0001c0025t0001g0120 a0004c0032t0001g0254 |
2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2860-1480T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150386422 | |||||||
chr5:150386535 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2860-1367G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150386535 | |||||||
chr5:150386588 | C | G | 4 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 others(1): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860-1314C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150386588 | |||||||
chr5:150386612 | CAG | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0034 others(28): Show |
44 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.2860-1286_2860-128 others(6): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr5 | 150386612 | ||||||
chr5:150386822 | T | C | 1 | a0004c0004t0007g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2860-1080T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150386822 | |||||||
chr5:150386869 | C | T | 1 | a0022c0018t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2860-1033C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150386869 | |||||||
chr5:150386982 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2860-920C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150386982 | |||||||
chr5:150387092 | A | G | 4 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 others(1): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860-810A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387092 | |||||||
chr5:150387203 | T | C | 1 | a0004c0004t0007g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2860-699T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387203 | |||||||
chr5:150387227 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
138 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.2860-675G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387227 | |||||||
chr5:150387246 | C | T | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2860-656C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387246 | |||||||
chr5:150387247 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2860-655G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387247 | |||||||
chr5:150387341 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2860-561G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387341 | |||||||
chr5:150387396 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2860-506T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387396 | |||||||
chr5:150387520 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(158): Show |
219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.2860-382T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387520 | |||||||
chr5:150387531 | GC | G | 19 | a0004c0004t0001g0017 a0004c0004t0001g0024 a0004c0004t0001g0025 others(16): Show |
24 | HG01099.hp2 HG01167.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2860-369delC | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr5 | 150387531 | ||||||
chr5:150387534 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
133 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.2860-368G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387534 | |||||||
chr5:150387731 | A | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0001g0102 others(3): Show |
7 | HG01256.hp1 HG01258.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.2860-171A>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387731 | |||||||
chr5:150387842 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2860-60C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387842 | |||||||
chr5:150387881 | G | A | 1 | a0023c0030t0001g0186 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2860-21G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 17/26 | chr5 | 150387881 | |||||||
chr5:150388271 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3046+183G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150388271 | |||||||
chr5:150388550 | T | C | 4 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(1): Show |
4 | HG03491.hp2 HG03669.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046+462T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150388550 | |||||||
chr5:150388613 | A | G | 1 | a0001c0001t0008g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3046+525A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150388613 | |||||||
chr5:150388659 | C | A | 1 | a0001c0001t0008g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3046+571C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150388659 | |||||||
chr5:150388758 | C | T | 4 | a0001c0001t0001g0159 a0005c0005t0001g0216 a0005c0005t0001g0244 others(1): Show |
4 | HG00642.hp2 HG02698.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.3046+670C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150388758 | |||||||
chr5:150388772 | T | C | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3046+684T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150388772 | |||||||
chr5:150388818 | G | A | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.3046+730G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150388818 | |||||||
chr5:150388893 | G | C | 2 | a0004c0004t0001g0017 a0004c0019t0001g0188 |
4 | HG03209.hp1 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046+805G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150388893 | |||||||
chr5:150388909 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3046+821G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150388909 | |||||||
chr5:150389186 | C | T | 2 | a0009c0014t0001g0207 a0009c0014t0001g0221 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3047-701C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150389186 | |||||||
chr5:150389267 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0138 others(6): Show |
12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.3047-620T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150389267 | |||||||
chr5:150389314 | C | T | 46 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(43): Show |
63 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.3047-573C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150389314 | |||||||
chr5:150389345 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0222 |
2 | HG02129.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.3047-542C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150389345 | |||||||
chr5:150389346 | A | G | 6 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(3): Show |
7 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3047-541A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150389346 | |||||||
chr5:150389575 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0133 |
3 | NA18942.hp1 NA18981.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3047-312G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150389575 | |||||||
chr5:150389775 | C | G | 1 | a0001c0001t0001g0141 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3047-112C>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150389775 | |||||||
chr5:150389867 | C | T | 1 | a0004c0004t0007g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3047-20C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 18/26 | chr5 | 150389867 | |||||||
chr5:150390091 | A | G | 6 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(3): Show |
7 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3183+68A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 19/26 | chr5 | 150390091 | |||||||
chr5:150390125 | G | C | 23 | a0004c0004t0001g0017 a0004c0004t0001g0022 a0004c0004t0001g0024 others(20): Show |
29 | HG01099.hp2 HG01167.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.3183+102G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 19/26 | chr5 | 150390125 | |||||||
chr5:150390180 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3183+157A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 19/26 | chr5 | 150390180 | |||||||
chr5:150390292 | G | A | 1 | a0013c0013t0001g0124 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3183+269G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 19/26 | chr5 | 150390292 | |||||||
chr5:150390495 | C | T | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.3183+472C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 19/26 | chr5 | 150390495 | |||||||
chr5:150391031 | G | C | 1 | a0004c0004t0007g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3184-513G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 19/26 | chr5 | 150391031 | |||||||
chr5:150391063 | C | T | 6 | a0003c0003t0002g0007 a0003c0003t0002g0011 a0003c0003t0002g0066 others(3): Show |
11 | HG00140.hp1 HG00673.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.3184-481C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 19/26 | chr5 | 150391063 | |||||||
chr5:150391178 | G | A | 3 | a0001c0001t0001g0152 a0012c0017t0001g0103 a0012c0017t0001g0215 |
3 | HG02572.hp2 HG03041.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.3184-366G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 19/26 | chr5 | 150391178 | |||||||
chr5:150391343 | C | T | 3 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 |
4 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3184-201C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 19/26 | chr5 | 150391343 | |||||||
chr5:150391690 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3297+33C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 20/26 | chr5 | 150391690 | |||||||
chr5:150391716 | C | T | 1 | a0009c0014t0001g0221 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3297+59C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 20/26 | chr5 | 150391716 | |||||||
chr5:150391723 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0034 others(27): Show |
43 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.3297+66C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 20/26 | chr5 | 150391723 | |||||||
chr5:150392232 | T | C | 1 | a0019c0029t0001g0125 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3517+56T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 21/26 | chr5 | 150392232 | |||||||
chr5:150392340 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0119 |
3 | HG02717.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3517+164A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 21/26 | chr5 | 150392340 | |||||||
chr5:150392654 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3518-51C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 21/26 | chr5 | 150392654 | |||||||
chr5:150392674 | G | A | 22 | a0004c0004t0001g0017 a0004c0004t0001g0022 a0004c0004t0001g0024 others(19): Show |
28 | HG01099.hp2 HG01167.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.3518-31G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 21/26 | chr5 | 150392674 | |||||||
chr5:150392976 | G | A | 1 | a0015c0024t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3603+186G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 22/26 | chr5 | 150392976 | |||||||
chr5:150393017 | T | G | 1 | a0002c0002t0001g0058 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3603+227T>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 22/26 | chr5 | 150393017 | |||||||
chr5:150393051 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3603+261G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 22/26 | chr5 | 150393051 | |||||||
chr5:150393155 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3604-217T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 22/26 | chr5 | 150393155 | |||||||
chr5:150393200 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG01106.hp1 HG01952.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.3604-172C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 22/26 | chr5 | 150393200 | |||||||
chr5:150393358 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3604-14A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 22/26 | chr5 | 150393358 | |||||||
chr5:150393369 | C | T | 18 | a0004c0004t0001g0017 a0004c0004t0001g0022 a0004c0004t0001g0024 others(15): Show |
24 | HG01099.hp2 HG01167.hp1 HG01361.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.3604-3C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 22/26 | chr5 | 150393369 | |||||||
chr5:150393654 | G | T | 1 | a0015c0024t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3784+102G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150393654 | |||||||
chr5:150393771 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3784+219T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150393771 | |||||||
chr5:150394037 | G | C | 1 | a0003c0003t0002g0071 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3784+485G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394037 | |||||||
chr5:150394148 | G | A | 1 | a0002c0002t0001g0173 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3784+596G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394148 | |||||||
chr5:150394235 | T | A | 45 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(42): Show |
62 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.3784+683T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394235 | |||||||
chr5:150394386 | T | C | 2 | a0006c0006t0001g0039 a0006c0006t0002g0039 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3784+834T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394386 | |||||||
chr5:150394507 | G | A | 3 | a0008c0008t0001g0045 a0008c0008t0001g0219 a0008c0008t0001g0220 |
4 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3784+955G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394507 | |||||||
chr5:150394731 | A | G | 6 | a0006c0006t0001g0039 a0006c0006t0001g0189 a0006c0006t0001g0202 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3784+1179A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394731 | |||||||
chr5:150394776 | G | A | 12 | a0004c0004t0001g0024 a0004c0004t0001g0025 a0004c0004t0001g0041 others(9): Show |
15 | HG01099.hp2 HG01167.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.3784+1224G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394776 | |||||||
chr5:150394789 | C | T | 1 | a0009c0031t0001g0248 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3784+1237C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394789 | |||||||
chr5:150394879 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3784+1327C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394879 | |||||||
chr5:150394916 | C | CA | 47 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0028 others(44): Show |
63 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.3785-1342dupA | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr5 | 150394916 | ||||||
chr5:150394916 | C | CAA | 8 | a0003c0003t0001g0069 a0003c0003t0002g0011 a0003c0003t0002g0019 others(5): Show |
11 | HG00423.hp1 HG01361.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.3785-1343_3785-134 others(6): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr5 | 150394916 | ||||||
chr5:150394916 | CA | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(80): Show |
118 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.3785-1342delA | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr5 | 150394916 | ||||||
chr5:150394950 | A | G | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3785-1332A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394950 | |||||||
chr5:150394959 | G | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0117 |
2 | HG01496.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3785-1323G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394959 | |||||||
chr5:150394981 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3785-1301G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150394981 | |||||||
chr5:150395000 | A | T | 1 | a0003c0003t0002g0020 | 2 | HG02080.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.3785-1282A>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395000 | |||||||
chr5:150395067 | G | A | 1 | a0004c0004t0001g0022 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3785-1215G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395067 | |||||||
chr5:150395107 | A | T | 1 | a0004c0004t0001g0022 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3785-1175A>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395107 | |||||||
chr5:150395448 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0118 |
3 | HG00738.hp1 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3785-834C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395448 | |||||||
chr5:150395481 | A | G | 3 | a0001c0001t0001g0191 a0002c0002t0001g0169 a0002c0002t0001g0173 |
3 | HG00544.hp1 HG03041.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.3785-801A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395481 | |||||||
chr5:150395537 | G | GT | 10 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0099 others(7): Show |
10 | HG00597.hp2 HG01243.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3785-732dupT | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr5 | 150395537 | ||||||
chr5:150395550 | T | A | 1 | a0002c0002t0001g0031 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3785-732T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395550 | |||||||
chr5:150395719 | G | T | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3785-563G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395719 | |||||||
chr5:150395826 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0082 |
3 | HG02155.hp1 HG02523.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3785-456G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395826 | |||||||
chr5:150395871 | C | T | 2 | a0002c0002t0001g0031 a0002c0002t0001g0179 |
3 | HG01257.hp1 HG01258.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3785-411C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395871 | |||||||
chr5:150395885 | A | AG | 16 | a0003c0003t0001g0069 a0003c0003t0002g0007 a0003c0003t0002g0010 others(13): Show |
26 | HG00140.hp1 HG00423.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.3785-397_3785-396i others(3): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 23/26 | chr5 | 150395885 | |||||||
chr5:150396852 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4345+10C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150396852 | |||||||
chr5:150396858 | T | C | 1 | a0005c0005t0001g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4345+16T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150396858 | |||||||
chr5:150396954 | C | T | 1 | a0002c0002t0001g0178 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4345+112C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150396954 | |||||||
chr5:150396965 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4345+123C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150396965 | |||||||
chr5:150396979 | A | G | 2 | a0009c0014t0001g0207 a0009c0014t0001g0221 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.4345+137A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150396979 | |||||||
chr5:150397065 | A | C | 3 | a0002c0002t0001g0031 a0002c0002t0001g0179 a0018c0028t0001g0163 |
4 | HG01257.hp1 HG01258.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.4345+223A>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397065 | |||||||
chr5:150397116 | G | T | 1 | a0002c0002t0001g0224 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4345+274G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397116 | |||||||
chr5:150397130 | C | T | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4345+288C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397130 | |||||||
chr5:150397153 | C | CA | 25 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0003c0003t0001g0069 others(22): Show |
35 | HG00423.hp1 HG01099.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.4345+332dupA | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr5 | 150397153 | ||||||
chr5:150397153 | C | CAA | 14 | a0003c0003t0002g0007 a0003c0003t0002g0011 a0003c0003t0002g0066 others(11): Show |
20 | HG00140.hp1 HG00673.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.4345+331_4345+332d others(4): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr5 | 150397153 | ||||||
chr5:150397153 | C | CAAAA | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(50): Show |
76 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.4345+329_4345+332d others(6): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr5 | 150397153 | ||||||
chr5:150397153 | C | CAAAAA | 31 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0034 others(28): Show |
43 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.4345+328_4345+332d others(7): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr5 | 150397153 | ||||||
chr5:150397153 | C | CAAAAAA | 6 | a0001c0001t0001g0035 a0001c0001t0001g0144 a0001c0001t0001g0155 others(3): Show |
7 | HG00621.hp1 HG02015.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.4345+327_4345+332d others(8): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr5 | 150397153 | ||||||
chr5:150397153 | CA | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.4345+332delA | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr5 | 150397153 | ||||||
chr5:150397294 | T | A | 2 | a0002c0002t0001g0075 a0002c0002t0001g0198 |
2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.4345+452T>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397294 | |||||||
chr5:150397452 | T | TA | 6 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(3): Show |
7 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.4345+610_4345+611i others(3): Show |
TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397452 | |||||||
chr5:150397591 | C | T | 1 | a0022c0018t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4345+749C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397591 | |||||||
chr5:150397611 | A | G | 1 | a0002c0002t0001g0177 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4346-743A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397611 | |||||||
chr5:150397617 | G | A | 4 | a0006c0006t0001g0039 a0006c0006t0001g0189 a0006c0006t0001g0202 others(1): Show |
4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.4346-737G>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397617 | |||||||
chr5:150397652 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4346-702C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397652 | |||||||
chr5:150397678 | A | G | 1 | a0022c0018t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4346-676A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397678 | |||||||
chr5:150397687 | C | T | 6 | a0007c0007t0001g0051 a0007c0007t0001g0249 a0007c0007t0001g0250 others(3): Show |
7 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.4346-667C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397687 | |||||||
chr5:150397939 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0253 |
2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4346-415T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150397939 | |||||||
chr5:150398023 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4346-331A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150398023 | |||||||
chr5:150398049 | A | G | 7 | a0002c0002t0001g0038 a0002c0002t0001g0110 a0002c0002t0001g0111 others(4): Show |
8 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.4346-305A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150398049 | |||||||
chr5:150398072 | A | G | 1 | a0018c0028t0001g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4346-282A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150398072 | |||||||
chr5:150398161 | A | G | 7 | a0001c0001t0001g0204 a0007c0007t0001g0051 a0007c0007t0001g0249 others(4): Show |
8 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4346-193A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150398161 | |||||||
chr5:150398168 | C | T | 2 | a0006c0006t0001g0039 a0006c0006t0002g0039 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4346-186C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150398168 | |||||||
chr5:150398215 | C | T | 17 | a0004c0004t0001g0017 a0004c0004t0001g0024 a0004c0004t0001g0025 others(14): Show |
22 | HG01099.hp2 HG01167.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4346-139C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 24/26 | chr5 | 150398215 | |||||||
chr5:150398559 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4443+108C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 25/26 | chr5 | 150398559 | |||||||
chr5:150398571 | G | C | 1 | a0004c0004t0007g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4443+120G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 25/26 | chr5 | 150398571 | |||||||
chr5:150398797 | C | T | 2 | a0002c0002t0001g0038 a0002c0002t0001g0184 |
3 | HG01516.hp2 HG01993.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.4444-225C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 25/26 | chr5 | 150398797 | |||||||
chr5:150398801 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.4444-221G>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 25/26 | chr5 | 150398801 | |||||||
chr5:150398802 | C | T | 4 | a0003c0003t0002g0065 a0003c0003t0002g0067 a0003c0010t0002g0062 others(1): Show |
4 | HG03942.hp2 NA18940.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.4444-220C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 25/26 | chr5 | 150398802 | |||||||
chr5:150398890 | C | A | 20 | a0001c0001t0008g0063 a0004c0004t0001g0017 a0004c0004t0001g0024 others(17): Show |
25 | HG01099.hp2 HG01167.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.4444-132C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 25/26 | chr5 | 150398890 | |||||||
chr5:150399096 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0081 others(4): Show |
10 | HG01884.hp1 HG02451.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.*22+26A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399096 | |||||||
chr5:150399101 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.*22+31G>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399101 | |||||||
chr5:150399274 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0150 |
2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.*22+204T>C | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399274 | |||||||
chr5:150399320 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0234 |
3 | HG01496.hp2 HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.*22+250A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399320 | |||||||
chr5:150399368 | C | T | 2 | a0012c0017t0001g0103 a0012c0017t0001g0215 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.*22+298C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399368 | |||||||
chr5:150399393 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.*22+323C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399393 | |||||||
chr5:150399467 | C | T | 19 | a0004c0004t0001g0017 a0004c0004t0001g0024 a0004c0004t0001g0025 others(16): Show |
24 | HG01099.hp2 HG01167.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.*23-343C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399467 | |||||||
chr5:150399502 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0157 |
2 | NA19005.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.*23-308A>G | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399502 | |||||||
chr5:150399579 | C | T | 12 | a0004c0004t0001g0024 a0004c0004t0001g0025 a0004c0004t0001g0041 others(9): Show |
15 | HG01099.hp2 HG01167.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.*23-231C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399579 | |||||||
chr5:150399630 | C | A | 1 | a0004c0004t0001g0024 | 2 | HG01099.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.*23-180C>A | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399630 | |||||||
chr5:150399800 | C | T | 1 | a0005c0005t0001g0050 | 2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.*23-10C>T | TCOF1 | ENSG00000070814.22 | transcript | ENST00000643257.2 | protein_coding | 26/26 | chr5 | 150399800 |