Item | Value |
---|---|
geneid | 7047 |
ensemblid | ENSG00000163810.13 |
hgncid | 11780 |
symbol | TGM4 |
name | transglutaminase 4 |
refseq_nuc | NM_003241.4 |
refseq_prot | NP_003232.2 |
ensembl_nuc | ENST00000296125.9 |
ensembl_prot | ENSP00000296125.4 |
mane_status | MANE Select |
chr | chr3 |
start | 44874608 |
end | 44914990 |
strand | + |
ver | v1.2 |
region | chr3:44874608-44914990 |
region5000 | chr3:44869608-44919990 |
regionname0 | TGM4_chr3_44874608_44914990 |
regionname5000 | TGM4_chr3_44869608_44919990 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 684 | 86 | 9 | 18 | 43 | 2 | 14 | 27 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0002 | 1/1 | 684 | 84 | 18 | 28 | 20 | 7 | 9 | 16 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0003 | 0/0 | 684 | 40 | 14 | 5 | 9 | 1 | 11 | 5 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0004 | 0/0 | 684 | 31 | 4 | 13 | 8 | 4 | 2 | 7 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0005 | 0/0 | 684 | 15 | 12 | 2 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0006 | 0/0 | 684 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0007 | 0/0 | 684 | 7 | 4 | 2 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0008 | 0/0 | 684 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0009 | 0/0 | 684 | 6 | 5 | 0 | 1 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0010 | 0/0 | 684 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0011 | 0/0 | 684 | 5 | 4 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0012 | 0/0 | 684 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0013 | 0/0 | 684 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0014 | 0/0 | 684 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0015 | 0/0 | 684 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0016 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0017 | 0/0 | 268 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(263): Show |
chr3 | 44869608 | 44919990 |
a0018 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0019 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0020 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0021 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0022 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0023 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0024 | 0/0 | 268 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(263): Show |
chr3 | 44869608 | 44919990 |
a0025 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
a0026 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | MMDAS others(679): Show |
chr3 | 44869608 | 44919990 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2052 | 83 | 9 | 18 | 40 | 2 | 14 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0001c0014 | 0/0 | 2052 | 3 | 0 | 0 | 3 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0002c0002 | 1/1 | 2052 | 79 | 15 | 26 | 20 | 7 | 9 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0002c0013 | 0/0 | 2052 | 3 | 3 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0002c0018 | 0/0 | 2052 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0003c0003 | 0/0 | 2052 | 36 | 10 | 5 | 9 | 1 | 11 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0003c0012 | 0/0 | 2052 | 4 | 4 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0004c0004 | 0/0 | 2052 | 30 | 4 | 13 | 7 | 4 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0004c0023 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0005c0005 | 0/0 | 2052 | 15 | 12 | 2 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0006c0010 | 0/0 | 2052 | 5 | 5 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0006c0015 | 0/0 | 2052 | 3 | 3 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0007c0007 | 0/0 | 2052 | 7 | 4 | 2 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0008c0006 | 0/0 | 2052 | 7 | 7 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0009c0009 | 0/0 | 2052 | 6 | 5 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0010c0008 | 0/0 | 2052 | 6 | 0 | 0 | 6 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0011c0011 | 0/0 | 2052 | 5 | 4 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0012c0019 | 0/0 | 2052 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0013c0016 | 0/0 | 2052 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0014c0020 | 0/0 | 2052 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0015c0017 | 0/0 | 2052 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0016c0021 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0017c0022 | 0/0 | 2052 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0018c0028 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0019c0025 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0020c0024 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0021c0030 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0022c0032 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0023c0027 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0024c0029 | 0/0 | 2052 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0025c0026 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 | ||
a0026c0031 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ATGAT others(2047): Show |
chr3 | 44869608 | 44919990 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3391 | 83 | 9 | 18 | 40 | 2 | 14 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0001c0014t0001 | 0/0 | 3391 | 3 | 0 | 0 | 3 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0002c0002t0002 | 1/1 | 3391 | 76 | 13 | 25 | 20 | 7 | 9 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0002c0002t0007 | 0/0 | 3391 | 3 | 2 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0002c0013t0001 | 0/0 | 3391 | 3 | 3 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0002c0018t0002 | 0/0 | 3391 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0003c0003t0001 | 0/0 | 3391 | 36 | 10 | 5 | 9 | 1 | 11 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0003c0012t0001 | 0/0 | 3391 | 4 | 4 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0004c0004t0001 | 0/0 | 3391 | 30 | 4 | 13 | 7 | 4 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0004c0023t0001 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0005c0005t0001 | 0/0 | 3391 | 12 | 12 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0005c0005t0006 | 0/0 | 3391 | 3 | 0 | 2 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0006c0010t0003 | 0/0 | 3391 | 5 | 5 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0006c0015t0003 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0006c0015t0005 | 0/0 | 3391 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0007c0007t0001 | 0/0 | 3391 | 6 | 3 | 2 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0007c0007t0008 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(2667): Show |
chr3 | 44869608 | 44919990 |
a0008c0006t0003 | 0/0 | 3391 | 7 | 7 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0009c0009t0003 | 0/0 | 3391 | 5 | 4 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0009c0009t0005 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0010c0008t0004 | 0/0 | 3391 | 6 | 0 | 0 | 6 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0011c0011t0001 | 0/0 | 3391 | 5 | 4 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0012c0019t0002 | 0/0 | 3391 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0013c0016t0002 | 0/0 | 3391 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0014c0020t0001 | 0/0 | 3391 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0015c0017t0001 | 0/0 | 3391 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0016c0021t0001 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0017c0022t0001 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0018c0028t0001 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0019c0025t0003 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0020c0024t0001 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0021c0030t0003 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0022c0032t0001 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0023c0027t0002 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0024c0029t0001 | 0/0 | 3391 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0025c0026t0001 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
a0026c0031t0001 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | ACCGA others(3386): Show |
chr3 | 44869608 | 44919990 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0014t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0014t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0007g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0007g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0013t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0013t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0013t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0018t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0012t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0012t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0012t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0012t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0023t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0010t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0010t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0010t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0010t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0015t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0015t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0015t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0007t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0007t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0007t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0007t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0007t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0007t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0006t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0006t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0006t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0006t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0006t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0006t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0009t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0009t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0009t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0009t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0009t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0009t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0008t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0008t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0008t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0008t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0008t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0008t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0012c0019t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0012c0019t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0013c0016t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0013c0016t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0014c0020t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0014c0020t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0015c0017t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0015c0017t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0016c0021t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0017c0022t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0018c0028t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0019c0025t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0020c0024t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0021c0030t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0022c0032t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0023c0027t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0024c0029t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0025c0026t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0026c0031t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0007 | c0007 | t0001 | g0062 | EUR | GBR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00099 | hp2 | a0004 | c0004 | t0001 | g0228 | EUR | GBR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0270 | EUR | GBR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0115 | EUR | GBR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0028 | EUR | FIN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0106 | EUR | FIN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0054 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00639 | hp1 | a0004 | c0004 | t0001 | g0124 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00639 | hp2 | a0004 | c0004 | t0001 | g0143 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00642 | hp2 | a0005 | c0005 | t0006 | g0042 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00673 | hp2 | a0016 | c0021 | t0001 | g0151 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0086 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00741 | hp1 | a0007 | c0007 | t0001 | g0210 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00741 | hp2 | a0012 | c0019 | t0002 | g0128 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01070 | hp2 | a0004 | c0004 | t0001 | g0229 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01071 | hp1 | a0004 | c0004 | t0001 | g0026 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0119 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0131 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01074 | hp2 | a0004 | c0004 | t0001 | g0026 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01099 | hp1 | a0004 | c0004 | t0001 | g0233 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01099 | hp2 | a0004 | c0004 | t0001 | g0234 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01106 | hp1 | a0004 | c0004 | t0001 | g0144 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0220 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01109 | hp2 | a0007 | c0007 | t0001 | g0044 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01167 | hp1 | a0017 | c0022 | t0001 | g0236 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01167 | hp2 | a0002 | c0018 | t0002 | g0006 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01169 | hp2 | a0002 | c0018 | t0002 | g0006 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0105 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01192 | hp2 | a0005 | c0005 | t0006 | g0132 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01255 | hp1 | a0013 | c0016 | t0002 | g0247 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0031 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01256 | hp2 | a0004 | c0004 | t0001 | g0145 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0053 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0260 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01515 | hp2 | a0004 | c0004 | t0001 | g0232 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01516 | hp1 | a0004 | c0004 | t0001 | g0142 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01517 | hp2 | a0004 | c0004 | t0001 | g0231 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0136 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01884 | hp2 | a0008 | c0006 | t0003 | g0016 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01891 | hp1 | a0003 | c0012 | t0001 | g0104 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01891 | hp2 | a0003 | c0003 | t0001 | g0135 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0055 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0091 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01943 | hp2 | a0004 | c0004 | t0001 | g0248 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0272 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01975 | hp1 | a0013 | c0016 | t0002 | g0063 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01993 | hp2 | a0004 | c0004 | t0001 | g0249 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0085 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02055 | hp2 | a0018 | c0028 | t0001 | g0113 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02056 | hp2 | a0019 | c0025 | t0003 | g0181 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02071 | hp1 | a0001 | c0014 | t0001 | g0219 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02074 | hp2 | a0003 | c0003 | t0001 | g0060 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02129 | hp1 | a0001 | c0014 | t0001 | g0024 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02132 | hp2 | a0003 | c0003 | t0001 | g0076 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02135 | hp2 | a0003 | c0003 | t0001 | g0064 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02145 | hp1 | a0012 | c0019 | t0002 | g0125 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02145 | hp2 | a0005 | c0005 | t0001 | g0012 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02148 | hp1 | a0004 | c0004 | t0001 | g0251 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02257 | hp1 | a0008 | c0006 | t0003 | g0048 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02258 | hp1 | a0005 | c0005 | t0001 | g0116 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02258 | hp2 | a0009 | c0009 | t0005 | g0254 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02273 | hp1 | a0004 | c0004 | t0001 | g0250 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0056 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02280 | hp1 | a0003 | c0003 | t0001 | g0089 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02280 | hp2 | a0003 | c0012 | t0001 | g0108 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02300 | hp1 | a0002 | c0002 | t0007 | g0263 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02300 | hp2 | a0003 | c0003 | t0001 | g0097 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02523 | hp1 | a0004 | c0023 | t0001 | g0238 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02572 | hp1 | a0020 | c0024 | t0001 | g0194 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02572 | hp2 | a0004 | c0004 | t0001 | g0279 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02602 | hp1 | a0004 | c0004 | t0001 | g0216 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0118 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02615 | hp2 | a0004 | c0004 | t0001 | g0255 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02622 | hp1 | a0007 | c0007 | t0001 | g0043 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02622 | hp2 | a0005 | c0005 | t0001 | g0093 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02630 | hp1 | a0002 | c0013 | t0001 | g0155 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0265 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0141 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0057 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0262 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0052 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02717 | hp2 | a0002 | c0013 | t0001 | g0153 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02723 | hp1 | a0005 | c0005 | t0001 | g0101 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02723 | hp2 | a0008 | c0006 | t0003 | g0049 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02809 | hp1 | a0011 | c0011 | t0001 | g0037 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02809 | hp2 | a0005 | c0005 | t0001 | g0015 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02818 | hp1 | a0006 | c0015 | t0005 | g0121 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02818 | hp2 | a0021 | c0030 | t0003 | g0259 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02886 | hp1 | a0008 | c0006 | t0003 | g0274 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02895 | hp1 | a0005 | c0005 | t0001 | g0123 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02895 | hp2 | a0011 | c0011 | t0001 | g0039 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02896 | hp1 | a0011 | c0011 | t0001 | g0038 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02896 | hp2 | a0002 | c0002 | t0007 | g0027 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02897 | hp1 | a0002 | c0002 | t0007 | g0027 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02897 | hp2 | a0005 | c0005 | t0001 | g0122 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02922 | hp1 | a0003 | c0012 | t0001 | g0107 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02922 | hp2 | a0014 | c0020 | t0001 | g0040 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0140 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02965 | hp2 | a0011 | c0011 | t0001 | g0035 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02970 | hp1 | a0005 | c0005 | t0001 | g0012 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02970 | hp2 | a0003 | c0003 | t0001 | g0030 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02976 | hp2 | a0009 | c0009 | t0003 | g0152 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0059 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0134 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03041 | hp2 | a0008 | c0006 | t0003 | g0050 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0271 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03098 | hp2 | a0006 | c0010 | t0003 | g0068 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0273 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03130 | hp2 | a0022 | c0032 | t0001 | g0034 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03139 | hp1 | a0009 | c0009 | t0003 | g0258 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03139 | hp2 | a0008 | c0006 | t0003 | g0016 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0264 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03209 | hp2 | a0007 | c0007 | t0001 | g0099 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03225 | hp2 | a0004 | c0004 | t0001 | g0278 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0069 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03453 | hp1 | a0009 | c0009 | t0003 | g0257 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03486 | hp1 | a0008 | c0006 | t0003 | g0051 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03486 | hp2 | a0006 | c0015 | t0003 | g0130 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0275 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03491 | hp2 | a0003 | c0003 | t0001 | g0008 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0008 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03516 | hp1 | a0005 | c0005 | t0001 | g0100 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03516 | hp2 | a0006 | c0010 | t0003 | g0065 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03540 | hp2 | a0006 | c0015 | t0005 | g0120 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03654 | hp1 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0103 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03669 | hp1 | a0005 | c0005 | t0006 | g0126 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03669 | hp2 | a0004 | c0004 | t0001 | g0171 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0261 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03710 | hp1 | a0003 | c0003 | t0001 | g0276 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0112 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0066 | SAS | STU | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0058 | SAS | STU | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04184 | hp2 | a0003 | c0003 | t0001 | g0070 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0072 | SAS | STU | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18522 | hp2 | a0009 | c0009 | t0003 | g0256 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18612 | hp1 | a0015 | c0017 | t0001 | g0160 | EAS | CHB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0277 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0137 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18942 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18948 | hp1 | a0004 | c0004 | t0001 | g0209 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18964 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18964 | hp2 | a0004 | c0004 | t0001 | g0235 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18970 | hp1 | a0009 | c0009 | t0003 | g0253 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18975 | hp1 | a0010 | c0008 | t0004 | g0178 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18977 | hp1 | a0015 | c0017 | t0001 | g0176 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18978 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18981 | hp1 | a0004 | c0004 | t0001 | g0237 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0139 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18984 | hp1 | a0010 | c0008 | t0004 | g0157 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18991 | hp1 | a0010 | c0008 | t0004 | g0154 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18991 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18998 | hp2 | a0010 | c0008 | t0004 | g0242 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19003 | hp1 | a0010 | c0008 | t0004 | g0189 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0269 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19030 | hp2 | a0007 | c0007 | t0001 | g0082 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19043 | hp1 | a0007 | c0007 | t0008 | g0133 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19043 | hp2 | a0003 | c0003 | t0001 | g0080 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19056 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19063 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19063 | hp2 | a0001 | c0014 | t0001 | g0024 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19065 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19068 | hp2 | a0010 | c0008 | t0004 | g0149 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19077 | hp1 | a0023 | c0027 | t0002 | g0013 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19077 | hp2 | a0004 | c0004 | t0001 | g0252 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0268 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19240 | hp2 | a0005 | c0005 | t0001 | g0102 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20129 | hp1 | a0014 | c0020 | t0001 | g0036 | AFR | ASW | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20129 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | ASW | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0090 | EUR | TSI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20752 | hp2 | a0003 | c0003 | t0001 | g0074 | EUR | TSI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20805 | hp1 | a0011 | c0011 | t0001 | g0033 | EUR | TSI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0111 | EUR | TSI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20905 | hp2 | a0024 | c0029 | t0001 | g0117 | SAS | GIH | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02109 | hp2 | a0005 | c0005 | t0001 | g0015 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02486 | hp1 | a0002 | c0013 | t0001 | g0165 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02486 | hp2 | a0004 | c0004 | t0001 | g0240 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02559 | hp2 | a0006 | c0010 | t0003 | g0047 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03471 | hp2 | a0003 | c0012 | t0001 | g0087 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG06807 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | USA | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG06807 | hp2 | a0006 | c0010 | t0003 | g0007 | AFR | USA | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20300 | hp1 | a0006 | c0010 | t0003 | g0007 | AFR | USA | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20300 | hp2 | a0005 | c0005 | t0001 | g0129 | AFR | USA | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA21309 | hp1 | a0025 | c0026 | t0001 | g0222 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA21309 | hp2 | a0026 | c0031 | t0001 | g0041 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0046 | REF | REF | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0267 | REF | REF | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44887795 | G | C | 9 | a0001 a0004 a0010 others(6): Show |
131 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(128): Show |
missense_variant&splice_region_variant | MODERATE | c.300G>C | p.Glu100Asp | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/14 | 371/3391 | 300/2055 | 100/684 | chr3 | 44887795 | |||
chr3:44893589 | T | C | 1 | a0016 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.443T>C | p.Phe148Ser | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/14 | 514/3391 | 443/2055 | 148/684 | chr3 | 44893589 | |||
chr3:44893613 | A | G | 4 | a0011 a0014 a0022 others(1): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
missense_variant | MODERATE | c.467A>G | p.Lys156Arg | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/14 | 538/3391 | 467/2055 | 156/684 | chr3 | 44893613 | |||
chr3:44896799 | A | G | 1 | a0021 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.640A>G | p.Arg214Gly | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/14 | 711/3391 | 640/2055 | 214/684 | chr3 | 44896799 | |||
chr3:44901596 | T | C | 5 | a0006 a0008 a0009 others(2): Show |
23 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(20): Show |
missense_variant | MODERATE | c.730T>C | p.Tyr244His | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 801/3391 | 730/2055 | 244/684 | chr3 | 44901596 | |||
chr3:44901612 | G | C | 3 | a0004 a0017 a0024 |
33 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
missense_variant | MODERATE | c.746G>C | p.Ser249Thr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 817/3391 | 746/2055 | 249/684 | chr3 | 44901612 | |||
chr3:44901672 | G | A | 2 | a0017 a0024 |
2 | HG01167.hp1 NA20905.hp2 |
stop_gained | HIGH | c.806G>A | p.Trp269* | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 877/3391 | 806/2055 | 269/684 | chr3 | 44901672 | |||
chr3:44901897 | G | A | 15 | a0001 a0004 a0005 others(12): Show |
164 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(161): Show |
missense_variant | MODERATE | c.937G>A | p.Glu313Lys | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/14 | 1008/3391 | 937/2055 | 313/684 | chr3 | 44901897 | |||
chr3:44901907 | C | A | 1 | a0010 | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
missense_variant | MODERATE | c.947C>A | p.Thr316Asn | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/14 | 1018/3391 | 947/2055 | 316/684 | chr3 | 44901907 | |||
chr3:44903951 | C | A | 1 | a0025 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1039C>A | p.Gln347Lys | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/14 | 1110/3391 | 1039/2055 | 347/684 | chr3 | 44903951 | |||
chr3:44906987 | C | T | 18 | a0001 a0003 a0004 others(15): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
missense_variant | MODERATE | c.1114C>T | p.Arg372Cys | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1185/3391 | 1114/2055 | 372/684 | chr3 | 44906987 | |||
chr3:44906988 | G | A | 1 | a0003 | 4 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.1115G>A | p.Arg372His | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1186/3391 | 1115/2055 | 372/684 | chr3 | 44906988 | |||
chr3:44906999 | A | G | 2 | a0011 a0018 |
6 | HG02055.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
missense_variant | MODERATE | c.1126A>G | p.Ile376Val | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1197/3391 | 1126/2055 | 376/684 | chr3 | 44906999 | |||
chr3:44907026 | G | A | 2 | a0010 a0023 |
7 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(4): Show |
missense_variant | MODERATE | c.1153G>A | p.Val385Ile | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1224/3391 | 1153/2055 | 385/684 | chr3 | 44907026 | |||
chr3:44907098 | G | A | 13 | a0001 a0003 a0004 others(10): Show |
189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
missense_variant | MODERATE | c.1225G>A | p.Val409Ile | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1296/3391 | 1225/2055 | 409/684 | chr3 | 44907098 | |||
chr3:44907125 | G | A | 1 | a0020 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1252G>A | p.Gly418Arg | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1323/3391 | 1252/2055 | 418/684 | chr3 | 44907125 | |||
chr3:44907182 | G | C | 2 | a0005 a0026 |
16 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(13): Show |
missense_variant | MODERATE | c.1309G>C | p.Glu437Gln | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1380/3391 | 1309/2055 | 437/684 | chr3 | 44907182 | |||
chr3:44913586 | C | T | 1 | a0008 | 7 | HG01884.hp2 HG02257.hp1 HG02723.hp2 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.1916C>T | p.Thr639Met | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 1987/3391 | 1916/2055 | 639/684 | chr3 | 44913586 | |||
chr3:44914271 | CAGTTTGA others(1426): Show |
C | 1 | a0007 | 1 | NA19043.hp1 | splice_region_variant | LOW | c.*547_*1979del | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | chr3 | 44914271 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44885368 | C | T | 1 | a0006c0015 | 3 | HG02818.hp1 HG03486.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.63C>T | p.Ala21Ala | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/14 | 134/3391 | 63/2055 | 21/684 | chr3 | 44885368 | |||
chr3:44887747 | A | G | 1 | a0001c0014 | 3 | HG02071.hp1 HG02129.hp1 NA19063.hp2 |
synonymous_variant | LOW | c.252A>G | p.Ser84Ser | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/14 | 323/3391 | 252/2055 | 84/684 | chr3 | 44887747 | |||
chr3:44893617 | G | A | 4 | a0011c0011 a0014c0020 a0022c0032 others(1): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
synonymous_variant | LOW | c.471G>A | p.Glu157Glu | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/14 | 542/3391 | 471/2055 | 157/684 | chr3 | 44893617 | |||
chr3:44901577 | C | T | 19 | a0001c0001 a0001c0014 a0004c0004 others(16): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
synonymous_variant | LOW | c.711C>T | p.Tyr237Tyr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 782/3391 | 711/2055 | 237/684 | chr3 | 44901577 | |||
chr3:44901637 | C | T | 1 | a0026c0031 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.771C>T | p.Tyr257Tyr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 842/3391 | 771/2055 | 257/684 | chr3 | 44901637 | |||
chr3:44907055 | C | T | 1 | a0006c0010 | 5 | HG02559.hp2 HG03098.hp2 HG03516.hp2 others(2): Show |
synonymous_variant | LOW | c.1182C>T | p.Leu394Leu | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1253/3391 | 1182/2055 | 394/684 | chr3 | 44907055 | |||
chr3:44907115 | C | A | 1 | a0026c0031 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1242C>A | p.Thr414Thr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1313/3391 | 1242/2055 | 414/684 | chr3 | 44907115 | |||
chr3:44907124 | C | T | 1 | a0002c0018 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1251C>T | p.Ile417Ile | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1322/3391 | 1251/2055 | 417/684 | chr3 | 44907124 | |||
chr3:44910178 | T | C | 1 | a0004c0023 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.1416T>C | p.Phe472Phe | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/14 | 1487/3391 | 1416/2055 | 472/684 | chr3 | 44910178 | |||
chr3:44913719 | C | T | 1 | a0002c0013 | 3 | HG02486.hp1 HG02630.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.2049C>T | p.Thr683Thr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 2120/3391 | 2049/2055 | 683/684 | chr3 | 44913719 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44913726 | C | G | 1 | a0002c0002t0007 | 3 | HG02300.hp1 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 1 | chr3 | 44913726 | ||||||
chr3:44913912 | G | A | 8 | a0006c0010t0003 a0006c0015t0003 a0006c0015t0005 others(5): Show |
23 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*187G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 187 | chr3 | 44913912 | ||||||
chr3:44913943 | G | A | 2 | a0006c0015t0005 a0009c0009t0005 |
3 | HG02258.hp2 HG02818.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*218G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 218 | chr3 | 44913943 | ||||||
chr3:44914001 | T | A | 1 | a0005c0005t0006 | 3 | HG00642.hp2 HG01192.hp2 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*276T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 276 | chr3 | 44914001 | ||||||
chr3:44914038 | G | T | 31 | a0001c0001t0001 a0001c0014t0001 a0002c0013t0001 others(28): Show |
228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*313G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 313 | chr3 | 44914038 | ||||||
chr3:44914090 | C | T | 1 | a0010c0008t0004 | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*365C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 365 | chr3 | 44914090 | ||||||
chr3:44914353 | C | T | 1 | a0001c0001t0001 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*628C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 628 | chr3 | 44914353 | ||||||
chr3:44914406 | A | G | 1 | a0003c0003t0001 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 681 | chr3 | 44914406 | ||||||
chr3:44914486 | T | C | 2 | a0002c0013t0001 a0025c0026t0001 |
4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*761T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 761 | chr3 | 44914486 | ||||||
chr3:44914606 | G | C | 2 | a0009c0009t0003 a0019c0025t0003 |
6 | HG02056.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*881G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 881 | chr3 | 44914606 | ||||||
chr3:44914678 | G | C | 1 | a0001c0001t0001 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 953 | chr3 | 44914678 | ||||||
chr3:44914748 | A | G | 3 | a0001c0001t0001 a0003c0003t0001 a0019c0025t0003 |
5 | HG01496.hp2 HG02056.hp2 HG02273.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1023A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 1023 | chr3 | 44914748 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44874719 | G | A | 1 | a0002c0018t0002g0006 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.19+22G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44874719 | |||||||
chr3:44874741 | C | A | 2 | a0002c0002t0002g0031 a0002c0002t0002g0032 |
2 | HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.19+44C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44874741 | |||||||
chr3:44874907 | G | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+210G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44874907 | |||||||
chr3:44875099 | G | A | 251 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(248): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.19+402G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875099 | |||||||
chr3:44875189 | T | G | 1 | a0005c0005t0006g0042 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.19+492T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875189 | |||||||
chr3:44875198 | C | A | 2 | a0007c0007t0001g0043 a0007c0007t0001g0044 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.19+501C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875198 | |||||||
chr3:44875302 | T | C | 1 | a0003c0003t0001g0045 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.19+605T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875302 | |||||||
chr3:44875619 | C | T | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19+922C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875619 | |||||||
chr3:44875639 | A | C | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+942A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875639 | |||||||
chr3:44875802 | T | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1105T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875802 | |||||||
chr3:44875966 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1269A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875966 | |||||||
chr3:44876009 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1312C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876009 | |||||||
chr3:44876036 | G | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1339G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876036 | |||||||
chr3:44876184 | A | G | 16 | a0004c0004t0001g0255 a0009c0009t0003g0253 a0009c0009t0003g0256 others(13): Show |
16 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.19+1487A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876184 | |||||||
chr3:44876196 | C | G | 2 | a0004c0004t0001g0004 a0004c0004t0001g0252 |
4 | NA18942.hp2 NA19056.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+1499C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876196 | |||||||
chr3:44876243 | A | G | 125 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(122): Show |
136 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.19+1546A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876243 | |||||||
chr3:44876358 | C | A | 38 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0057 others(35): Show |
43 | HG00099.hp1 HG00609.hp1 HG01358.hp2 others(40): Show |
intron_variant | MODIFIER | c.19+1661C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876358 | |||||||
chr3:44876365 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1668A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876365 | |||||||
chr3:44876383 | G | A | 1 | a0003c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+1686G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876383 | |||||||
chr3:44876421 | C | A | 4 | a0004c0004t0001g0142 a0004c0004t0001g0143 a0004c0004t0001g0144 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+1724C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876421 | |||||||
chr3:44876465 | TGATATGT others(9): Show |
T | 1 | a0001c0001t0001g0146 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.19+1769_19+1784del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876465 | |||||||
chr3:44876720 | TAAAGGA | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2028_19+2033del others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44876720 | ||||||
chr3:44876989 | A | G | 1 | a0002c0002t0002g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.19+2292A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876989 | |||||||
chr3:44877275 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2578C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877275 | |||||||
chr3:44877429 | G | T | 33 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0057 others(30): Show |
38 | HG00099.hp1 HG00609.hp1 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.19+2732G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877429 | |||||||
chr3:44877457 | T | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2760T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877457 | |||||||
chr3:44877477 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2780A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877477 | |||||||
chr3:44877569 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.19+2872G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877569 | |||||||
chr3:44877593 | T | TA | 6 | a0002c0002t0002g0083 a0004c0004t0001g0142 a0004c0004t0001g0143 others(3): Show |
6 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+2908dupA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44877593 | ||||||
chr3:44877593 | TA | T | 11 | a0002c0002t0002g0140 a0003c0003t0001g0139 a0004c0004t0001g0251 others(8): Show |
11 | HG02148.hp1 HG02809.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+2908delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44877593 | ||||||
chr3:44877761 | A | AT | 5 | a0001c0001t0001g0246 a0004c0004t0001g0248 a0004c0004t0001g0249 others(2): Show |
5 | HG01255.hp1 HG01943.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+3067dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44877761 | ||||||
chr3:44877917 | G | A | 44 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0057 others(41): Show |
49 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.19+3220G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877917 | |||||||
chr3:44878345 | A | G | 1 | a0002c0002t0002g0138 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.19+3648A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878345 | |||||||
chr3:44878378 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18952.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.19+3681T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878378 | |||||||
chr3:44878444 | T | TTTA | 3 | a0011c0011t0001g0033 a0011c0011t0001g0038 a0011c0011t0001g0039 |
3 | HG02895.hp2 HG02896.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.19+3749_19+3750ins others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878444 | ||||||
chr3:44878447 | G | A | 248 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(245): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.19+3750G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878447 | |||||||
chr3:44878447 | G | T | 3 | a0011c0011t0001g0033 a0011c0011t0001g0038 a0011c0011t0001g0039 |
3 | HG02895.hp2 HG02896.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.19+3750G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878447 | |||||||
chr3:44878449 | T | TTTA | 17 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0085 others(14): Show |
23 | HG00735.hp2 HG00738.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.19+3800_19+3802dup others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | ||||||
chr3:44878449 | TTTA | T | 36 | a0002c0002t0002g0014 a0002c0002t0002g0057 a0002c0002t0002g0083 others(33): Show |
37 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.19+3800_19+3802del others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | ||||||
chr3:44878449 | TTTATTA | T | 27 | a0001c0001t0001g0019 a0001c0001t0001g0156 a0001c0001t0001g0158 others(24): Show |
28 | HG00099.hp1 HG00408.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.19+3797_19+3802del others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | ||||||
chr3:44878449 | TTTATTAT others(2): Show |
T | 55 | a0001c0001t0001g0020 a0001c0001t0001g0127 a0001c0001t0001g0146 others(52): Show |
63 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.19+3794_19+3802del others(9): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | ||||||
chr3:44878449 | TTTATTAT others(5): Show |
T | 68 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
73 | HG00609.hp2 HG00733.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.19+3791_19+3802del others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | ||||||
chr3:44878449 | TTTATTAT others(8): Show |
T | 22 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0003c0003t0001g0080 others(19): Show |
25 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.19+3788_19+3802del others(15): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | ||||||
chr3:44878449 | TTTATTAT others(11): Show |
T | 9 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+3785_19+3802del others(18): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | ||||||
chr3:44878452 | A | T | 2 | a0011c0011t0001g0035 a0014c0020t0001g0036 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.19+3755A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878452 | |||||||
chr3:44878455 | A | T | 1 | a0014c0020t0001g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19+3758A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878455 | |||||||
chr3:44878461 | A | T | 1 | a0026c0031t0001g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19+3764A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878461 | |||||||
chr3:44878508 | G | T | 3 | a0011c0011t0001g0037 a0011c0011t0001g0038 a0011c0011t0001g0039 |
3 | HG02809.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.19+3811G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878508 | |||||||
chr3:44878543 | C | T | 46 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(43): Show |
53 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.19+3846C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878543 | |||||||
chr3:44878631 | C | G | 1 | a0003c0003t0001g0066 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19+3934C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878631 | |||||||
chr3:44878632 | G | A | 46 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(43): Show |
53 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.19+3935G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878632 | |||||||
chr3:44878768 | C | T | 1 | a0006c0015t0003g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.19+4071C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878768 | |||||||
chr3:44878943 | T | C | 5 | a0003c0003t0001g0017 a0003c0003t0001g0135 a0003c0003t0001g0136 others(2): Show |
6 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+4246T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878943 | |||||||
chr3:44879025 | C | T | 1 | a0002c0013t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19+4328C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879025 | |||||||
chr3:44879058 | G | C | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19+4361G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879058 | |||||||
chr3:44879066 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.19+4369T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879066 | |||||||
chr3:44879237 | G | GTC | 6 | a0005c0005t0001g0012 a0005c0005t0001g0101 a0005c0005t0001g0102 others(3): Show |
7 | HG02145.hp2 HG02723.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+4568_19+4569dup others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879237 | ||||||
chr3:44879237 | GTC | G | 14 | a0001c0001t0001g0241 a0002c0018t0002g0006 a0003c0003t0001g0017 others(11): Show |
16 | HG01167.hp2 HG01169.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.19+4568_19+4569del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879237 | ||||||
chr3:44879237 | GTCTC | G | 41 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0156 others(38): Show |
44 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.19+4566_19+4569del others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879237 | ||||||
chr3:44879253 | CTCTCTCT others(9): Show |
C | 1 | a0022c0032t0001g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.19+4558_19+4573del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879253 | ||||||
chr3:44879255 | CTCTCTCT others(5): Show |
C | 1 | a0008c0006t0003g0016 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19+4560_19+4571del others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879255 | ||||||
chr3:44879255 | CTCTCTCT others(9): Show |
C | 3 | a0011c0011t0001g0035 a0011c0011t0001g0038 a0011c0011t0001g0039 |
3 | HG02895.hp2 HG02896.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.19+4560_19+4575del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879255 | ||||||
chr3:44879257 | C | A | 1 | a0002c0002t0002g0002 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.19+4560C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879257 | |||||||
chr3:44879257 | CTCTCTCT others(5): Show |
C | 1 | a0006c0010t0003g0047 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19+4562_19+4573del others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879257 | ||||||
chr3:44879257 | CTCTCTCT others(9): Show |
C | 4 | a0011c0011t0001g0037 a0014c0020t0001g0036 a0014c0020t0001g0040 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+4562_19+4577del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879257 | ||||||
chr3:44879259 | C | A | 4 | a0002c0002t0002g0002 a0002c0002t0002g0103 a0002c0002t0002g0140 others(1): Show |
4 | HG02129.hp2 HG02965.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4562C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879259 | |||||||
chr3:44879259 | CTCTCTCT others(1): Show |
C | 18 | a0002c0002t0002g0010 a0002c0002t0002g0011 a0002c0002t0002g0057 others(15): Show |
21 | HG01358.hp2 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.19+4564_19+4571del others(8): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879259 | ||||||
chr3:44879259 | CTCTCTCT others(9): Show |
C | 1 | a0011c0011t0001g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.19+4564_19+4579del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879259 | ||||||
chr3:44879261 | C | A | 10 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0103 others(7): Show |
10 | HG00140.hp1 HG01071.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+4564C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879261 | |||||||
chr3:44879261 | C | CTATA | 3 | a0002c0002t0002g0028 a0002c0002t0002g0031 a0002c0002t0002g0260 |
3 | HG00735.hp1 HG01256.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.19+4565_19+4566ins others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879261 | ||||||
chr3:44879261 | CTCTCTAT others(1): Show |
C | 10 | a0002c0002t0002g0071 a0002c0002t0002g0073 a0002c0002t0002g0084 others(7): Show |
10 | HG00408.hp1 HG01975.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+4566_19+4573del others(8): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879261 | ||||||
chr3:44879263 | C | A | 34 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(31): Show |
39 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.19+4566C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879263 | |||||||
chr3:44879263 | C | CTA | 3 | a0002c0013t0001g0165 a0005c0005t0001g0100 a0007c0007t0001g0044 |
3 | HG01109.hp2 HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+4567_19+4568ins others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | ||||||
chr3:44879263 | C | CTATA | 4 | a0002c0002t0002g0005 a0002c0002t0002g0014 a0002c0002t0002g0028 others(1): Show |
5 | HG00280.hp1 HG01106.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4567_19+4568ins others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | ||||||
chr3:44879263 | C | CTATATA | 3 | a0002c0002t0002g0105 a0002c0002t0002g0110 a0003c0003t0001g0276 |
3 | HG01168.hp2 HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.19+4567_19+4568ins others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | ||||||
chr3:44879263 | CTCTA | C | 39 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0023 others(36): Show |
41 | HG00558.hp2 HG00673.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.19+4568_19+4571del others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | ||||||
chr3:44879263 | CTCTATAT others(1): Show |
C | 4 | a0003c0003t0001g0054 a0003c0003t0001g0076 a0006c0010t0003g0007 others(1): Show |
5 | HG00609.hp1 HG02132.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4568_19+4575del others(8): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | ||||||
chr3:44879265 | C | A | 70 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0172 others(67): Show |
83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.19+4568C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879265 | |||||||
chr3:44879265 | C | CTA | 8 | a0001c0001t0001g0127 a0002c0002t0002g0134 a0002c0013t0001g0153 others(5): Show |
9 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4589_19+4590dup others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | ||||||
chr3:44879265 | C | CTATA | 4 | a0002c0002t0002g0083 a0002c0002t0002g0261 a0005c0005t0001g0116 others(1): Show |
4 | HG01496.hp1 HG02258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4587_19+4590dup others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | ||||||
chr3:44879265 | C | CTATATA | 3 | a0002c0002t0002g0262 a0002c0002t0002g0275 a0002c0002t0007g0263 |
3 | HG02300.hp1 HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.19+4585_19+4590dup others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | ||||||
chr3:44879265 | C | CTCTCTAT others(3): Show |
1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19+4569_19+4570ins others(10): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | ||||||
chr3:44879265 | CTA | C | 4 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0001g0226 others(1): Show |
4 | HG02056.hp1 HG02145.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+4589_19+4590del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | ||||||
chr3:44879265 | CTATA | C | 40 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(37): Show |
43 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.19+4587_19+4590del others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | ||||||
chr3:44879267 | A | C | 7 | a0002c0002t0002g0081 a0002c0002t0002g0118 a0003c0012t0001g0104 others(4): Show |
7 | HG01891.hp1 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+4570A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879267 | |||||||
chr3:44879269 | A | C | 5 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0003c0012t0001g0108 others(2): Show |
5 | HG02056.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4572A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879269 | |||||||
chr3:44879271 | A | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0164 a0001c0001t0001g0223 others(6): Show |
10 | HG01952.hp2 HG02055.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+4574A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879271 | |||||||
chr3:44879273 | A | C | 1 | a0001c0001t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.19+4576A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879273 | |||||||
chr3:44879286 | T | G | 1 | a0002c0002t0002g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.19+4589T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879286 | |||||||
chr3:44879309 | T | A | 168 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(165): Show |
184 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.19+4612T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879309 | |||||||
chr3:44879313 | T | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0227 |
2 | HG03710.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.19+4616T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879313 | |||||||
chr3:44879388 | C | CCTCTGCC others(159): Show |
2 | a0002c0002t0002g0114 a0002c0002t0002g0115 |
2 | HG00140.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.19+4757_19+4758ins others(166): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879388 | ||||||
chr3:44879455 | T | C | 253 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(250): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.19+4758T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879455 | |||||||
chr3:44879470 | C | CTTTT | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4774_19+4775ins others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879470 | ||||||
chr3:44879472 | A | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4775A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879472 | |||||||
chr3:44879473 | A | AT | 7 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0003c0003t0001g0080 others(4): Show |
7 | HG01361.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+4793dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879473 | ||||||
chr3:44879473 | A | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4776A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879473 | |||||||
chr3:44879473 | AT | A | 7 | a0001c0001t0001g0146 a0004c0004t0001g0255 a0009c0009t0003g0152 others(4): Show |
7 | HG02258.hp2 HG02615.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+4793delT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879473 | ||||||
chr3:44879511 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0245 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.19+4814C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879511 | |||||||
chr3:44879666 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4969C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879666 | |||||||
chr3:44879819 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+5122A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879819 | |||||||
chr3:44880028 | G | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-5297G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880028 | |||||||
chr3:44880058 | C | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-5267C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880058 | |||||||
chr3:44880074 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.20-5251T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880074 | |||||||
chr3:44880433 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4892C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880433 | |||||||
chr3:44880470 | C | T | 1 | a0002c0002t0002g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.20-4855C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880470 | |||||||
chr3:44880542 | G | T | 5 | a0009c0009t0003g0253 a0009c0009t0003g0256 a0009c0009t0003g0257 others(2): Show |
5 | HG02258.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-4783G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880542 | |||||||
chr3:44880649 | A | C | 124 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(121): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.20-4676A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880649 | |||||||
chr3:44880654 | T | C | 3 | a0002c0013t0001g0153 a0002c0013t0001g0155 a0002c0013t0001g0165 |
3 | HG02486.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.20-4671T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880654 | |||||||
chr3:44880669 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.20-4656A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880669 | |||||||
chr3:44880698 | T | C | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4627T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880698 | |||||||
chr3:44880987 | G | A | 2 | a0004c0004t0001g0251 a0008c0006t0003g0050 |
2 | HG02148.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.20-4338G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880987 | |||||||
chr3:44880997 | C | T | 1 | a0003c0003t0001g0139 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.20-4328C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880997 | |||||||
chr3:44880998 | G | A | 5 | a0009c0009t0003g0253 a0009c0009t0003g0256 a0009c0009t0003g0257 others(2): Show |
5 | HG02258.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-4327G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880998 | |||||||
chr3:44881055 | T | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4270T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881055 | |||||||
chr3:44881057 | T | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4268T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881057 | |||||||
chr3:44881058 | G | A | 10 | a0003c0003t0001g0059 a0011c0011t0001g0033 a0011c0011t0001g0035 others(7): Show |
10 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-4267G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881058 | |||||||
chr3:44881060 | A | ATAAAAAA others(5): Show |
9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4265_20-4264ins others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881060 | |||||||
chr3:44881063 | GCA | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4260_20-4259del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44881063 | ||||||
chr3:44881066 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4259C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881066 | |||||||
chr3:44881067 | T | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4258T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881067 | |||||||
chr3:44881068 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4257A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881068 | |||||||
chr3:44881100 | A | T | 1 | a0020c0024t0001g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.20-4225A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881100 | |||||||
chr3:44881146 | G | A | 1 | a0004c0004t0001g0278 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.20-4179G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881146 | |||||||
chr3:44881243 | C | G | 4 | a0006c0015t0003g0130 a0006c0015t0005g0120 a0006c0015t0005g0121 others(1): Show |
5 | HG01884.hp2 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-4082C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881243 | |||||||
chr3:44881357 | T | C | 3 | a0004c0004t0001g0255 a0004c0004t0001g0278 a0004c0004t0001g0279 |
3 | HG02572.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.20-3968T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881357 | |||||||
chr3:44881366 | T | C | 2 | a0002c0002t0002g0031 a0002c0002t0002g0032 |
2 | HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.20-3959T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881366 | |||||||
chr3:44881533 | G | A | 1 | a0003c0003t0001g0067 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.20-3792G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881533 | |||||||
chr3:44881576 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.20-3749C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881576 | |||||||
chr3:44881597 | G | A | 1 | a0003c0003t0001g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.20-3728G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881597 | |||||||
chr3:44881696 | C | T | 1 | a0022c0032t0001g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.20-3629C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881696 | |||||||
chr3:44881852 | G | C | 1 | a0020c0024t0001g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.20-3473G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881852 | |||||||
chr3:44881856 | C | A | 1 | a0001c0001t0001g0223 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.20-3469C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881856 | |||||||
chr3:44881911 | G | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-3414G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881911 | |||||||
chr3:44882049 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.20-3276T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882049 | |||||||
chr3:44882057 | C | CT | 90 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(87): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.20-3247dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | ||||||
chr3:44882057 | C | CTT | 18 | a0002c0002t0002g0079 a0002c0002t0002g0092 a0002c0002t0002g0098 others(15): Show |
18 | HG02055.hp2 HG02074.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.20-3248_20-3247dup others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | ||||||
chr3:44882057 | C | CTTT | 18 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0003c0003t0001g0064 others(15): Show |
20 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.20-3249_20-3247dup others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | ||||||
chr3:44882057 | C | CTTTT | 87 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(84): Show |
97 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.20-3250_20-3247dup others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | ||||||
chr3:44882057 | C | CTTTTT | 38 | a0001c0001t0001g0020 a0001c0001t0001g0163 a0001c0001t0001g0170 others(35): Show |
39 | HG00408.hp1 HG00673.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.20-3251_20-3247dup others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | ||||||
chr3:44882136 | A | G | 2 | a0002c0002t0002g0275 a0003c0003t0001g0276 |
2 | HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.20-3189A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882136 | |||||||
chr3:44882295 | G | T | 1 | a0003c0003t0001g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.20-3030G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882295 | |||||||
chr3:44882367 | G | C | 15 | a0009c0009t0003g0253 a0009c0009t0003g0256 a0009c0009t0003g0257 others(12): Show |
15 | HG02258.hp2 HG02809.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-2958G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882367 | |||||||
chr3:44882414 | C | T | 4 | a0003c0003t0001g0017 a0003c0003t0001g0135 a0003c0003t0001g0136 others(1): Show |
5 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-2911C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882414 | |||||||
chr3:44882488 | A | C | 4 | a0004c0004t0001g0142 a0004c0004t0001g0143 a0004c0004t0001g0144 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-2837A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882488 | |||||||
chr3:44882526 | G | A | 2 | a0002c0002t0002g0261 a0002c0002t0002g0270 |
2 | HG00140.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.20-2799G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882526 | |||||||
chr3:44882764 | C | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-2561C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882764 | |||||||
chr3:44882936 | G | A | 1 | a0003c0003t0001g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.20-2389G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882936 | |||||||
chr3:44883374 | G | T | 1 | a0009c0009t0003g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.20-1951G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883374 | |||||||
chr3:44883409 | G | A | 22 | a0001c0001t0001g0127 a0004c0004t0001g0124 a0005c0005t0001g0012 others(19): Show |
24 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.20-1916G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883409 | |||||||
chr3:44883571 | C | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1754C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883571 | |||||||
chr3:44883624 | C | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1701C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883624 | |||||||
chr3:44883704 | G | A | 1 | a0002c0002t0002g0085 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.20-1621G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883704 | |||||||
chr3:44883745 | C | T | 1 | a0002c0002t0002g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.20-1580C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883745 | |||||||
chr3:44883856 | T | C | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1469T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883856 | |||||||
chr3:44883913 | T | G | 1 | a0004c0004t0001g0249 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.20-1412T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883913 | |||||||
chr3:44883942 | G | T | 1 | a0003c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.20-1383G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883942 | |||||||
chr3:44883943 | T | A | 1 | a0002c0002t0002g0270 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.20-1382T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883943 | |||||||
chr3:44883982 | G | A | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.20-1343G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883982 | |||||||
chr3:44884071 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1254C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884071 | |||||||
chr3:44884113 | T | C | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1212T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884113 | |||||||
chr3:44884139 | C | A | 9 | a0006c0010t0003g0007 a0006c0010t0003g0047 a0006c0010t0003g0065 others(6): Show |
11 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-1186C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884139 | |||||||
chr3:44884498 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG02735.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.20-827T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884498 | |||||||
chr3:44884643 | C | A | 1 | a0005c0005t0001g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20-682C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884643 | |||||||
chr3:44884676 | T | C | 1 | a0025c0026t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-649T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884676 | |||||||
chr3:44884692 | G | A | 7 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-633G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884692 | |||||||
chr3:44884728 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.20-597C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884728 | |||||||
chr3:44884918 | T | C | 4 | a0003c0003t0001g0017 a0003c0003t0001g0135 a0003c0003t0001g0136 others(1): Show |
5 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-407T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884918 | |||||||
chr3:44884975 | A | C | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-350A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884975 | |||||||
chr3:44885196 | G | A | 4 | a0004c0004t0001g0026 a0004c0004t0001g0228 a0004c0004t0001g0229 others(1): Show |
5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-129G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44885196 | |||||||
chr3:44885230 | C | G | 1 | a0004c0004t0001g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.20-95C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44885230 | |||||||
chr3:44885565 | T | C | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.193+67T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44885565 | |||||||
chr3:44885675 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.193+177C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44885675 | |||||||
chr3:44886112 | G | A | 14 | a0002c0002t0002g0005 a0002c0002t0002g0028 a0002c0002t0002g0031 others(11): Show |
18 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.193+614G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886112 | |||||||
chr3:44886198 | G | C | 29 | a0002c0002t0002g0057 a0002c0002t0002g0071 a0002c0002t0002g0073 others(26): Show |
31 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.193+700G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886198 | |||||||
chr3:44886242 | G | A | 1 | a0022c0032t0001g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.193+744G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886242 | |||||||
chr3:44886249 | T | TAGG | 202 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.193+753_193+754ins others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 44886249 | ||||||
chr3:44886287 | G | T | 1 | a0003c0003t0001g0067 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.193+789G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886287 | |||||||
chr3:44886340 | CA | C | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.193+851delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 44886340 | ||||||
chr3:44886397 | C | T | 26 | a0005c0005t0001g0012 a0005c0005t0001g0015 a0005c0005t0001g0093 others(23): Show |
28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.193+899C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886397 | |||||||
chr3:44886782 | G | T | 2 | a0022c0032t0001g0034 a0026c0031t0001g0041 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.194-907G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886782 | |||||||
chr3:44886875 | C | T | 1 | a0008c0006t0003g0049 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.194-814C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886875 | |||||||
chr3:44886992 | T | C | 29 | a0002c0002t0002g0057 a0002c0002t0002g0071 a0002c0002t0002g0073 others(26): Show |
32 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.194-697T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886992 | |||||||
chr3:44887331 | G | A | 119 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(116): Show |
130 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.194-358G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44887331 | |||||||
chr3:44887394 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-295C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44887394 | |||||||
chr3:44887426 | G | A | 26 | a0005c0005t0001g0012 a0005c0005t0001g0015 a0005c0005t0001g0093 others(23): Show |
28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-263G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44887426 | |||||||
chr3:44887622 | G | A | 9 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0159 others(6): Show |
9 | HG00558.hp2 HG01978.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-67G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44887622 | |||||||
chr3:44888104 | C | A | 5 | a0003c0003t0001g0017 a0003c0003t0001g0135 a0003c0003t0001g0136 others(2): Show |
6 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+309C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888104 | |||||||
chr3:44888130 | C | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+335C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888130 | |||||||
chr3:44888228 | G | A | 26 | a0005c0005t0001g0012 a0005c0005t0001g0015 a0005c0005t0001g0093 others(23): Show |
28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.300+433G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888228 | |||||||
chr3:44888239 | T | C | 5 | a0003c0003t0001g0017 a0003c0003t0001g0135 a0003c0003t0001g0136 others(2): Show |
6 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+444T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888239 | |||||||
chr3:44888251 | G | A | 3 | a0004c0004t0001g0255 a0004c0004t0001g0278 a0004c0004t0001g0279 |
3 | HG02572.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.300+456G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888251 | |||||||
chr3:44888318 | C | A | 2 | a0003c0003t0001g0052 a0007c0007t0001g0210 |
2 | HG00741.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.300+523C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888318 | |||||||
chr3:44888419 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+624C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888419 | |||||||
chr3:44888522 | C | T | 119 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(116): Show |
130 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.300+727C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888522 | |||||||
chr3:44888544 | T | C | 1 | a0003c0003t0001g0086 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.300+749T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888544 | |||||||
chr3:44888825 | C | G | 1 | a0022c0032t0001g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.300+1030C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888825 | |||||||
chr3:44889170 | T | TA | 70 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(67): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.301-1399dupA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | T | TAA | 33 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0156 others(30): Show |
35 | HG00408.hp2 HG00673.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.301-1400_301-1399d others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | T | TAAA | 18 | a0001c0001t0001g0148 a0001c0001t0001g0159 a0001c0001t0001g0170 others(15): Show |
18 | HG01261.hp2 HG01978.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.301-1401_301-1399d others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | T | TAAAA | 11 | a0001c0001t0001g0147 a0001c0001t0001g0173 a0001c0001t0001g0184 others(8): Show |
12 | HG00558.hp2 HG01433.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.301-1402_301-1399d others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | T | TAAAAAAA others(5): Show |
2 | a0003c0003t0001g0017 a0003c0003t0001g0137 |
3 | HG02559.hp1 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.300+1398_301-1399d others(14): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | T | TAAAAAAA others(6): Show |
2 | a0003c0003t0001g0136 a0007c0007t0001g0099 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.300+1397_301-1399d others(15): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | T | TAAAAAAA others(7): Show |
1 | a0003c0003t0001g0135 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.300+1396_301-1399d others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | TA | T | 13 | a0001c0001t0001g0127 a0001c0001t0001g0208 a0001c0001t0001g0221 others(10): Show |
14 | HG01943.hp1 HG02004.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-1399delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | TAA | T | 9 | a0004c0004t0001g0232 a0006c0015t0003g0130 a0006c0015t0005g0120 others(6): Show |
10 | HG01515.hp2 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-1400_301-1399d others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | TAAAA | T | 5 | a0002c0002t0007g0027 a0004c0004t0001g0235 a0004c0004t0001g0240 others(2): Show |
6 | HG01167.hp1 HG02148.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-1402_301-1399d others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | TAAAAA | T | 21 | a0004c0004t0001g0004 a0004c0004t0001g0026 a0004c0004t0001g0124 others(18): Show |
24 | HG00639.hp1 HG01071.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.301-1403_301-1399d others(7): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | TAAAAAA | T | 28 | a0001c0001t0001g0239 a0004c0004t0001g0143 a0004c0004t0001g0209 others(25): Show |
31 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.300+1404_301-1399d others(8): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | TAAAAAAA others(3): Show |
T | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.300+1400_301-1399d others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889170 | TAAAAAAA others(11): Show |
T | 11 | a0001c0014t0001g0024 a0001c0014t0001g0219 a0011c0011t0001g0033 others(8): Show |
12 | HG02071.hp1 HG02129.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.300+1392_301-1399d others(20): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | ||||||
chr3:44889215 | G | A | 2 | a0006c0010t0003g0007 a0006c0010t0003g0065 |
3 | HG03516.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.301-1388G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889215 | |||||||
chr3:44889228 | C | T | 1 | a0022c0032t0001g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.301-1375C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889228 | |||||||
chr3:44889319 | C | T | 9 | a0003c0003t0001g0080 a0006c0010t0003g0047 a0006c0010t0003g0068 others(6): Show |
10 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.301-1284C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889319 | |||||||
chr3:44889332 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-1271A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889332 | |||||||
chr3:44889357 | A | ATCT | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-1244_301-1242d others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889357 | ||||||
chr3:44889607 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-996A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889607 | |||||||
chr3:44889722 | A | T | 120 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(117): Show |
131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.301-881A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889722 | |||||||
chr3:44889737 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0223 |
2 | HG02080.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.301-866C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889737 | |||||||
chr3:44889792 | GT | G | 13 | a0003c0003t0001g0017 a0003c0003t0001g0135 a0003c0003t0001g0136 others(10): Show |
14 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-802delT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889792 | ||||||
chr3:44889992 | C | G | 1 | a0003c0003t0001g0276 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.301-611C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889992 | |||||||
chr3:44890042 | A | C | 1 | a0001c0014t0001g0219 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.301-561A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890042 | |||||||
chr3:44890200 | C | T | 120 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(117): Show |
131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.301-403C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890200 | |||||||
chr3:44890447 | G | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-156G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890447 | |||||||
chr3:44890522 | C | T | 2 | a0001c0001t0001g0148 a0003c0003t0001g0008 |
3 | HG03491.hp2 HG03492.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.301-81C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890522 | |||||||
chr3:44890532 | T | C | 1 | a0003c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301-71T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890532 | |||||||
chr3:44890569 | G | C | 2 | a0003c0003t0001g0058 a0003c0003t0001g0070 |
2 | HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.301-34G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890569 | |||||||
chr3:44890778 | C | T | 85 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(82): Show |
93 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.430+46C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890778 | |||||||
chr3:44890797 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0202 |
2 | HG00609.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.430+65T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890797 | |||||||
chr3:44890816 | T | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+84T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890816 | |||||||
chr3:44890883 | A | C | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+151A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890883 | |||||||
chr3:44890908 | C | T | 3 | a0006c0015t0003g0130 a0006c0015t0005g0120 a0006c0015t0005g0121 |
3 | HG02818.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.430+176C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890908 | |||||||
chr3:44890959 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+227C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890959 | |||||||
chr3:44891009 | C | T | 1 | a0003c0003t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.430+277C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891009 | |||||||
chr3:44891368 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.430+636T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891368 | |||||||
chr3:44891370 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.430+638A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891370 | |||||||
chr3:44891371 | C | CCT | 203 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(200): Show |
221 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.430+639_430+640ins others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891371 | |||||||
chr3:44891442 | TATC | T | 130 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(127): Show |
141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.430+714_430+716del others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891442 | ||||||
chr3:44891512 | T | TAC | 9 | a0001c0001t0001g0197 a0007c0007t0001g0062 a0011c0011t0001g0033 others(6): Show |
9 | HG00099.hp1 HG02809.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+808_430+809dup others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891512 | ||||||
chr3:44891512 | TAC | T | 110 | a0001c0001t0001g0208 a0001c0001t0001g0221 a0001c0001t0001g0245 others(107): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.430+808_430+809del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891512 | ||||||
chr3:44891512 | TACAC | T | 72 | a0001c0001t0001g0127 a0001c0001t0001g0190 a0001c0001t0001g0239 others(69): Show |
79 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.430+806_430+809del others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891512 | ||||||
chr3:44891542 | A | C | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+810A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891542 | |||||||
chr3:44891560 | C | G | 120 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(117): Show |
131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.430+828C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891560 | |||||||
chr3:44891697 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+965A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891697 | |||||||
chr3:44891701 | G | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+969G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891701 | |||||||
chr3:44891757 | G | A | 1 | a0003c0003t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.430+1025G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891757 | |||||||
chr3:44891762 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.430+1030T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891762 | |||||||
chr3:44891763 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.430+1031G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891763 | |||||||
chr3:44891832 | G | A | 1 | a0004c0004t0001g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.430+1100G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891832 | |||||||
chr3:44891843 | C | T | 1 | a0002c0018t0002g0006 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.430+1111C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891843 | |||||||
chr3:44891847 | C | T | 2 | a0012c0019t0002g0125 a0012c0019t0002g0128 |
2 | HG00741.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.430+1115C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891847 | |||||||
chr3:44891963 | GA | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+1242delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891963 | ||||||
chr3:44891971 | A | G | 1 | a0002c0002t0002g0106 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.430+1239A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891971 | |||||||
chr3:44891986 | C | T | 29 | a0002c0002t0002g0057 a0002c0002t0002g0071 a0002c0002t0002g0073 others(26): Show |
31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.430+1254C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891986 | |||||||
chr3:44892119 | C | G | 205 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(202): Show |
224 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.430+1387C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892119 | |||||||
chr3:44892172 | C | T | 29 | a0002c0002t0002g0057 a0002c0002t0002g0071 a0002c0002t0002g0073 others(26): Show |
31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.431-1405C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892172 | |||||||
chr3:44892206 | T | C | 204 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(201): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.431-1371T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892206 | |||||||
chr3:44892207 | G | A | 1 | a0002c0002t0002g0075 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.431-1370G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892207 | |||||||
chr3:44892234 | G | A | 6 | a0009c0009t0003g0152 a0009c0009t0003g0253 a0009c0009t0003g0256 others(3): Show |
6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-1343G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892234 | |||||||
chr3:44892259 | A | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-1318A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892259 | |||||||
chr3:44892283 | A | T | 29 | a0002c0002t0002g0057 a0002c0002t0002g0071 a0002c0002t0002g0073 others(26): Show |
31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.431-1294A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892283 | |||||||
chr3:44892285 | T | A | 29 | a0002c0002t0002g0057 a0002c0002t0002g0071 a0002c0002t0002g0073 others(26): Show |
31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.431-1292T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892285 | |||||||
chr3:44892362 | AT | A | 137 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(134): Show |
148 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.431-1198delT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44892362 | ||||||
chr3:44892385 | G | A | 120 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(117): Show |
131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.431-1192G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892385 | |||||||
chr3:44892424 | G | A | 1 | a0004c0004t0001g0237 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.431-1153G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892424 | |||||||
chr3:44892434 | G | A | 2 | a0005c0005t0001g0122 a0005c0005t0001g0123 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-1143G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892434 | |||||||
chr3:44892576 | G | T | 20 | a0005c0005t0001g0012 a0005c0005t0001g0015 a0005c0005t0001g0093 others(17): Show |
22 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.431-1001G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892576 | |||||||
chr3:44892674 | C | T | 5 | a0004c0004t0001g0142 a0004c0004t0001g0143 a0004c0004t0001g0144 others(2): Show |
5 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-903C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892674 | |||||||
chr3:44892789 | T | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-788T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892789 | |||||||
chr3:44892790 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-787A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892790 | |||||||
chr3:44892831 | G | T | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.431-746G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892831 | |||||||
chr3:44892889 | A | G | 26 | a0005c0005t0001g0012 a0005c0005t0001g0015 a0005c0005t0001g0093 others(23): Show |
28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.431-688A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892889 | |||||||
chr3:44892929 | G | A | 29 | a0002c0002t0002g0057 a0002c0002t0002g0071 a0002c0002t0002g0073 others(26): Show |
31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.431-648G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892929 | |||||||
chr3:44893267 | C | G | 1 | a0004c0004t0001g0249 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.431-310C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893267 | |||||||
chr3:44893396 | G | A | 120 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(117): Show |
131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.431-181G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893396 | |||||||
chr3:44893404 | G | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-173G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893404 | |||||||
chr3:44893488 | T | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-89T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893488 | |||||||
chr3:44893527 | C | T | 83 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(80): Show |
91 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.431-50C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893527 | |||||||
chr3:44893753 | G | A | 1 | a0006c0015t0005g0120 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.549+58G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44893753 | |||||||
chr3:44893826 | A | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+131A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44893826 | |||||||
chr3:44893933 | C | CGGCTCTC others(13): Show |
178 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(175): Show |
193 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.549+257_549+258ins others(20): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44893933 | ||||||
chr3:44893945 | A | ACCCCCCA others(14): Show |
1 | a0001c0001t0001g0180 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.549+257_549+258ins others(21): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44893945 | ||||||
chr3:44893954 | A | G | 6 | a0009c0009t0003g0152 a0009c0009t0003g0253 a0009c0009t0003g0256 others(3): Show |
6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.549+259A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44893954 | |||||||
chr3:44893973 | T | C | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+278T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44893973 | |||||||
chr3:44894063 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.549+368C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894063 | |||||||
chr3:44894108 | C | T | 3 | a0004c0004t0001g0255 a0004c0004t0001g0278 a0004c0004t0001g0279 |
3 | HG02572.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.549+413C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894108 | |||||||
chr3:44894111 | G | A | 1 | a0019c0025t0003g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.549+416G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894111 | |||||||
chr3:44894114 | T | C | 1 | a0002c0002t0002g0277 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.549+419T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894114 | |||||||
chr3:44894171 | TCCCCCAT others(13): Show |
T | 8 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(5): Show |
8 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.549+532_549+551del others(20): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44894171 | ||||||
chr3:44894235 | C | G | 1 | a0001c0001t0001g0243 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.549+540C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894235 | |||||||
chr3:44894258 | T | C | 269 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(266): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.549+563T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894258 | |||||||
chr3:44894322 | C | G | 1 | a0008c0006t0003g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.549+627C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894322 | |||||||
chr3:44894329 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.549+634C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894329 | |||||||
chr3:44894440 | CAAGCACT others(9): Show |
C | 1 | a0007c0007t0001g0210 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.549+776_549+791del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44894440 | ||||||
chr3:44894465 | T | C | 5 | a0005c0005t0001g0015 a0005c0005t0001g0116 a0005c0005t0001g0122 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.549+770T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894465 | |||||||
chr3:44894512 | C | CT | 203 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(200): Show |
221 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.549+818dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44894512 | ||||||
chr3:44894578 | C | G | 20 | a0005c0005t0001g0012 a0005c0005t0001g0015 a0005c0005t0001g0093 others(17): Show |
22 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.549+883C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894578 | |||||||
chr3:44894593 | G | A | 29 | a0002c0002t0002g0057 a0002c0002t0002g0071 a0002c0002t0002g0073 others(26): Show |
31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.549+898G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894593 | |||||||
chr3:44894643 | C | G | 6 | a0009c0009t0003g0152 a0009c0009t0003g0253 a0009c0009t0003g0256 others(3): Show |
6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.549+948C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894643 | |||||||
chr3:44894660 | T | A | 1 | a0025c0026t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549+965T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894660 | |||||||
chr3:44894890 | C | G | 82 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(79): Show |
90 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.549+1195C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894890 | |||||||
chr3:44894938 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+1243C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894938 | |||||||
chr3:44894995 | C | T | 119 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(116): Show |
130 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.549+1300C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894995 | |||||||
chr3:44895166 | G | A | 6 | a0008c0006t0003g0016 a0008c0006t0003g0048 a0008c0006t0003g0049 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+1471G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895166 | |||||||
chr3:44895244 | G | T | 2 | a0001c0001t0001g0190 a0020c0024t0001g0194 |
2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.550-1465G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895244 | |||||||
chr3:44895310 | A | G | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550-1399A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895310 | |||||||
chr3:44895776 | G | A | 1 | a0002c0002t0002g0262 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.550-933G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895776 | |||||||
chr3:44895879 | G | A | 6 | a0009c0009t0003g0152 a0009c0009t0003g0253 a0009c0009t0003g0256 others(3): Show |
6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.550-830G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895879 | |||||||
chr3:44895901 | T | G | 6 | a0009c0009t0003g0152 a0009c0009t0003g0253 a0009c0009t0003g0256 others(3): Show |
6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.550-808T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895901 | |||||||
chr3:44896001 | C | T | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.550-708C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896001 | |||||||
chr3:44896124 | T | G | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.550-585T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896124 | |||||||
chr3:44896137 | G | A | 4 | a0004c0004t0001g0142 a0004c0004t0001g0143 a0004c0004t0001g0144 others(1): Show |
4 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-572G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896137 | |||||||
chr3:44896179 | T | C | 1 | a0010c0008t0004g0149 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.550-530T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896179 | |||||||
chr3:44896198 | G | A | 1 | a0003c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.550-511G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896198 | |||||||
chr3:44896214 | C | T | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550-495C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896214 | |||||||
chr3:44896268 | C | T | 28 | a0003c0003t0001g0060 a0003c0003t0001g0061 a0005c0005t0001g0012 others(25): Show |
30 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.550-441C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896268 | |||||||
chr3:44896273 | G | T | 1 | a0003c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.550-436G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896273 | |||||||
chr3:44896339 | G | A | 1 | a0002c0002t0002g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.550-370G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896339 | |||||||
chr3:44896355 | C | T | 2 | a0007c0007t0001g0043 a0007c0007t0001g0044 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.550-354C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896355 | |||||||
chr3:44896521 | C | T | 10 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(7): Show |
10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.550-188C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896521 | |||||||
chr3:44896631 | T | C | 1 | a0005c0005t0006g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.550-78T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896631 | |||||||
chr3:44896986 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.657+170G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44896986 | |||||||
chr3:44897000 | CT | C | 18 | a0001c0001t0001g0180 a0001c0001t0001g0205 a0001c0001t0001g0214 others(15): Show |
18 | HG01070.hp1 HG01167.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.657+205delT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 44897000 | ||||||
chr3:44897000 | CTT | C | 175 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(172): Show |
191 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.657+204_657+205del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 44897000 | ||||||
chr3:44897000 | CTTT | C | 13 | a0001c0001t0001g0150 a0001c0001t0001g0163 a0003c0003t0001g0052 others(10): Show |
15 | HG01168.hp1 HG01255.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.657+203_657+205del others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 44897000 | ||||||
chr3:44897007 | T | C | 4 | a0009c0009t0003g0152 a0009c0009t0003g0256 a0009c0009t0003g0257 others(1): Show |
4 | HG02976.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+191T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897007 | |||||||
chr3:44897047 | T | C | 10 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(7): Show |
10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+231T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897047 | |||||||
chr3:44897057 | G | A | 10 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(7): Show |
10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+241G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897057 | |||||||
chr3:44897058 | C | T | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.657+242C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897058 | |||||||
chr3:44897094 | A | C | 277 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(274): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.657+278A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897094 | |||||||
chr3:44897128 | C | T | 1 | a0006c0010t0003g0047 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.657+312C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897128 | |||||||
chr3:44897152 | A | G | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.657+336A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897152 | |||||||
chr3:44897154 | G | T | 10 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(7): Show |
10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+338G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897154 | |||||||
chr3:44897293 | C | T | 10 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(7): Show |
10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+477C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897293 | |||||||
chr3:44897295 | C | T | 1 | a0003c0012t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.657+479C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897295 | |||||||
chr3:44897628 | T | C | 58 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(55): Show |
67 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.657+812T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897628 | |||||||
chr3:44897770 | T | C | 10 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(7): Show |
10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+954T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897770 | |||||||
chr3:44897868 | G | T | 1 | a0003c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.657+1052G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897868 | |||||||
chr3:44897945 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.657+1129G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897945 | |||||||
chr3:44898064 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.657+1248G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898064 | |||||||
chr3:44898067 | G | A | 9 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.657+1251G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898067 | |||||||
chr3:44898096 | A | G | 120 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(117): Show |
131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.657+1280A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898096 | |||||||
chr3:44898239 | C | T | 2 | a0002c0002t0002g0131 a0002c0002t0002g0140 |
2 | HG01074.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.657+1423C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898239 | |||||||
chr3:44898257 | G | C | 1 | a0002c0002t0002g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.657+1441G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898257 | |||||||
chr3:44898275 | T | C | 10 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(7): Show |
10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+1459T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898275 | |||||||
chr3:44898280 | CA | C | 263 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(260): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.657+1482delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 44898280 | ||||||
chr3:44898358 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.657+1542C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898358 | |||||||
chr3:44898441 | T | C | 10 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(7): Show |
10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+1625T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898441 | |||||||
chr3:44898539 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.657+1723A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898539 | |||||||
chr3:44898615 | G | A | 10 | a0006c0010t0003g0007 a0006c0010t0003g0047 a0006c0010t0003g0065 others(7): Show |
12 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.657+1799G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898615 | |||||||
chr3:44898654 | G | C | 6 | a0009c0009t0003g0152 a0009c0009t0003g0253 a0009c0009t0003g0256 others(3): Show |
6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+1838G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898654 | |||||||
chr3:44898662 | C | T | 1 | a0022c0032t0001g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.657+1846C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898662 | |||||||
chr3:44898834 | C | T | 30 | a0001c0001t0001g0190 a0001c0001t0001g0239 a0004c0004t0001g0004 others(27): Show |
33 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.657+2018C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898834 | |||||||
chr3:44898921 | A | G | 147 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(144): Show |
160 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.657+2105A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898921 | |||||||
chr3:44899108 | A | G | 1 | a0025c0026t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.657+2292A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899108 | |||||||
chr3:44899110 | A | G | 30 | a0002c0002t0002g0057 a0002c0002t0002g0071 a0002c0002t0002g0073 others(27): Show |
32 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.657+2294A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899110 | |||||||
chr3:44899127 | C | G | 2 | a0011c0011t0001g0038 a0011c0011t0001g0039 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.657+2311C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899127 | |||||||
chr3:44899145 | G | A | 2 | a0004c0004t0001g0235 a0004c0023t0001g0238 |
2 | HG02523.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.657+2329G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899145 | |||||||
chr3:44899434 | C | T | 1 | a0016c0021t0001g0151 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.658-2090C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899434 | |||||||
chr3:44899489 | C | A | 1 | a0006c0015t0003g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.658-2035C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899489 | |||||||
chr3:44899566 | G | T | 3 | a0002c0002t0002g0105 a0002c0002t0002g0110 a0002c0002t0002g0119 |
3 | HG01071.hp2 HG01168.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.658-1958G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899566 | |||||||
chr3:44899643 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG02735.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.658-1881C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899643 | |||||||
chr3:44899658 | G | A | 35 | a0001c0001t0001g0127 a0001c0001t0001g0190 a0001c0001t0001g0208 others(32): Show |
38 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.658-1866G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899658 | |||||||
chr3:44899666 | T | A | 8 | a0002c0002t0002g0071 a0002c0002t0002g0073 a0003c0003t0001g0053 others(5): Show |
8 | HG01496.hp2 HG02074.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-1858T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899666 | |||||||
chr3:44899958 | C | T | 1 | a0003c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.658-1566C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899958 | |||||||
chr3:44899973 | G | A | 1 | a0021c0030t0003g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.658-1551G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899973 | |||||||
chr3:44900040 | C | A | 153 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(150): Show |
168 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.658-1484C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900040 | |||||||
chr3:44900090 | G | A | 6 | a0009c0009t0003g0152 a0009c0009t0003g0253 a0009c0009t0003g0256 others(3): Show |
6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-1434G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900090 | |||||||
chr3:44900368 | C | G | 162 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(159): Show |
177 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.658-1156C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900368 | |||||||
chr3:44900485 | A | G | 133 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(130): Show |
146 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.658-1039A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900485 | |||||||
chr3:44900629 | C | T | 167 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(164): Show |
183 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.658-895C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900629 | |||||||
chr3:44900845 | G | A | 162 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(159): Show |
177 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.658-679G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900845 | |||||||
chr3:44900991 | C | A | 6 | a0010c0008t0004g0149 a0010c0008t0004g0154 a0010c0008t0004g0157 others(3): Show |
6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-533C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900991 | |||||||
chr3:44901004 | T | C | 163 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(160): Show |
178 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.658-520T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901004 | |||||||
chr3:44901096 | C | T | 1 | a0007c0007t0001g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.658-428C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901096 | |||||||
chr3:44901182 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0150 a0007c0007t0001g0210 |
4 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-342G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901182 | |||||||
chr3:44901279 | T | C | 162 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(159): Show |
177 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.658-245T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901279 | |||||||
chr3:44901296 | G | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0202 |
2 | HG00609.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.658-228G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901296 | |||||||
chr3:44901315 | C | A | 7 | a0010c0008t0004g0149 a0010c0008t0004g0154 a0010c0008t0004g0157 others(4): Show |
7 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.658-209C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901315 | |||||||
chr3:44901315 | C | G | 167 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(164): Show |
183 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.658-209C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901315 | |||||||
chr3:44902083 | T | A | 6 | a0010c0008t0004g0149 a0010c0008t0004g0154 a0010c0008t0004g0157 others(3): Show |
6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.971+152T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902083 | |||||||
chr3:44902121 | T | C | 5 | a0003c0012t0001g0087 a0003c0012t0001g0104 a0003c0012t0001g0107 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+190T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902121 | |||||||
chr3:44902234 | T | C | 153 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(150): Show |
168 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.971+303T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902234 | |||||||
chr3:44902389 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.971+458G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902389 | |||||||
chr3:44902470 | C | T | 152 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(149): Show |
167 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.971+539C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902470 | |||||||
chr3:44902494 | G | A | 15 | a0005c0005t0001g0012 a0005c0005t0001g0015 a0005c0005t0001g0093 others(12): Show |
17 | HG00642.hp2 HG00741.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.971+563G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902494 | |||||||
chr3:44902663 | CCT | C | 155 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.971+735_971+736del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 44902663 | ||||||
chr3:44902908 | T | A | 3 | a0004c0004t0001g0255 a0004c0004t0001g0278 a0004c0004t0001g0279 |
3 | HG02572.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.972-976T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902908 | |||||||
chr3:44903064 | A | G | 155 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.972-820A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903064 | |||||||
chr3:44903128 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.972-756C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903128 | |||||||
chr3:44903251 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-633A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903251 | |||||||
chr3:44903289 | T | C | 155 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.972-595T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903289 | |||||||
chr3:44903351 | T | C | 1 | a0007c0007t0008g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.972-533T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903351 | |||||||
chr3:44903571 | C | T | 77 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(74): Show |
85 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.972-313C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903571 | |||||||
chr3:44903575 | T | C | 155 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.972-309T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903575 | |||||||
chr3:44903629 | G | A | 155 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.972-255G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903629 | |||||||
chr3:44903667 | C | T | 7 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-217C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903667 | |||||||
chr3:44903853 | C | T | 1 | a0003c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.972-31C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903853 | |||||||
chr3:44904099 | A | G | 1 | a0002c0018t0002g0006 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1075+112A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904099 | |||||||
chr3:44904202 | T | C | 1 | a0004c0004t0001g0233 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1075+215T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904202 | |||||||
chr3:44904233 | GGTT | G | 52 | a0002c0002t0002g0057 a0002c0002t0002g0075 a0003c0003t0001g0008 others(49): Show |
57 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+247_1075+249d others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904233 | |||||||
chr3:44904237 | C | T | 52 | a0002c0002t0002g0057 a0002c0002t0002g0075 a0003c0003t0001g0008 others(49): Show |
57 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+250C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904237 | |||||||
chr3:44904238 | C | A | 52 | a0002c0002t0002g0057 a0002c0002t0002g0075 a0003c0003t0001g0008 others(49): Show |
57 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+251C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904238 | |||||||
chr3:44904248 | A | G | 182 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(179): Show |
199 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1075+261A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904248 | |||||||
chr3:44904501 | C | T | 1 | a0017c0022t0001g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1075+514C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904501 | |||||||
chr3:44904608 | G | C | 12 | a0001c0001t0001g0190 a0003c0003t0001g0086 a0003c0003t0001g0089 others(9): Show |
12 | HG00738.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+621G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904608 | |||||||
chr3:44904676 | T | A | 1 | a0002c0002t0002g0260 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1075+689T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904676 | |||||||
chr3:44904918 | G | A | 1 | a0007c0007t0001g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1075+931G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904918 | |||||||
chr3:44905106 | T | C | 1 | a0003c0003t0001g0064 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1075+1119T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905106 | |||||||
chr3:44905279 | C | G | 1 | a0003c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1075+1292C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905279 | |||||||
chr3:44905291 | C | CT | 190 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(187): Show |
209 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1075+1316dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 44905291 | ||||||
chr3:44905753 | A | G | 172 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(169): Show |
189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1076-1196A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905753 | |||||||
chr3:44905838 | G | C | 193 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-1111G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905838 | |||||||
chr3:44905839 | C | CT | 193 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-1110_1076-110 others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905839 | |||||||
chr3:44905840 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1076-1109A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905840 | |||||||
chr3:44905954 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1076-995C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905954 | |||||||
chr3:44906062 | G | A | 193 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-887G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906062 | |||||||
chr3:44906129 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1076-820G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906129 | |||||||
chr3:44906142 | C | T | 193 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-807C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906142 | |||||||
chr3:44906265 | G | A | 6 | a0010c0008t0004g0149 a0010c0008t0004g0154 a0010c0008t0004g0157 others(3): Show |
6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076-684G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906265 | |||||||
chr3:44906378 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1076-571A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906378 | |||||||
chr3:44906466 | AACAGCTT others(15): Show |
A | 193 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-478_1076-457d others(24): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 44906466 | ||||||
chr3:44906519 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1076-430A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906519 | |||||||
chr3:44906542 | A | G | 6 | a0010c0008t0004g0149 a0010c0008t0004g0154 a0010c0008t0004g0157 others(3): Show |
6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076-407A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906542 | |||||||
chr3:44906562 | A | C | 1 | a0004c0004t0001g0237 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1076-387A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906562 | |||||||
chr3:44907278 | G | A | 172 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(169): Show |
189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1327+78G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907278 | |||||||
chr3:44907308 | A | G | 1 | a0002c0002t0002g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1327+108A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907308 | |||||||
chr3:44907310 | C | CA | 6 | a0002c0002t0002g0032 a0002c0002t0002g0077 a0002c0002t0002g0094 others(3): Show |
6 | HG00642.hp1 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1327+133dupA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | ||||||
chr3:44907310 | CA | C | 6 | a0002c0002t0002g0078 a0002c0002t0002g0084 a0002c0002t0002g0140 others(3): Show |
6 | HG00408.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1327+133delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | ||||||
chr3:44907310 | CAA | C | 15 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0001g0163 others(12): Show |
15 | HG00741.hp1 HG01361.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1327+132_1327+133d others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | ||||||
chr3:44907310 | CAAA | C | 77 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(74): Show |
86 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1327+131_1327+133d others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | ||||||
chr3:44907310 | CAAAA | C | 104 | a0001c0001t0001g0127 a0001c0001t0001g0208 a0001c0001t0001g0221 others(101): Show |
113 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.1327+130_1327+133d others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | ||||||
chr3:44907412 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1327+212G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907412 | |||||||
chr3:44907561 | T | G | 209 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(206): Show |
228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1327+361T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907561 | |||||||
chr3:44907618 | G | A | 1 | a0017c0022t0001g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1327+418G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907618 | |||||||
chr3:44907847 | T | C | 172 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(169): Show |
189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1327+647T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907847 | |||||||
chr3:44907866 | T | C | 1 | a0002c0002t0002g0032 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1327+666T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907866 | |||||||
chr3:44908000 | A | G | 21 | a0006c0010t0003g0007 a0006c0010t0003g0047 a0006c0010t0003g0065 others(18): Show |
23 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1327+800A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908000 | |||||||
chr3:44908244 | C | G | 21 | a0006c0010t0003g0007 a0006c0010t0003g0047 a0006c0010t0003g0065 others(18): Show |
23 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1327+1044C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908244 | |||||||
chr3:44908374 | G | GT | 24 | a0002c0002t0002g0077 a0006c0010t0003g0007 a0006c0010t0003g0047 others(21): Show |
26 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1327+1183dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44908374 | ||||||
chr3:44908375 | T | G | 2 | a0003c0003t0001g0080 a0025c0026t0001g0222 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1327+1175T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908375 | |||||||
chr3:44908413 | G | GT | 29 | a0002c0002t0002g0090 a0006c0010t0003g0007 a0006c0010t0003g0047 others(26): Show |
31 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1327+1221dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44908413 | ||||||
chr3:44908430 | A | C | 27 | a0006c0010t0003g0007 a0006c0010t0003g0047 a0006c0010t0003g0065 others(24): Show |
29 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1327+1230A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908430 | |||||||
chr3:44908503 | G | T | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0014c0020t0001g0036 others(1): Show |
4 | HG01109.hp2 HG02622.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327+1303G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908503 | |||||||
chr3:44908534 | T | G | 1 | a0011c0011t0001g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1327+1334T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908534 | |||||||
chr3:44908572 | A | AT | 172 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(169): Show |
189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1327+1373dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44908572 | ||||||
chr3:44908574 | A | C | 172 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(169): Show |
189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1327+1374A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908574 | |||||||
chr3:44908724 | C | T | 77 | a0001c0001t0001g0127 a0001c0001t0001g0190 a0001c0001t0001g0204 others(74): Show |
84 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1328-1366C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908724 | |||||||
chr3:44908757 | C | T | 193 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1328-1333C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908757 | |||||||
chr3:44908809 | T | G | 6 | a0010c0008t0004g0149 a0010c0008t0004g0154 a0010c0008t0004g0157 others(3): Show |
6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1328-1281T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908809 | |||||||
chr3:44908835 | C | T | 1 | a0002c0002t0002g0028 | 2 | HG00280.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1328-1255C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908835 | |||||||
chr3:44908873 | G | A | 1 | a0006c0010t0003g0047 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1328-1217G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908873 | |||||||
chr3:44909008 | A | G | 200 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(197): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1328-1082A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909008 | |||||||
chr3:44909403 | A | G | 209 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(206): Show |
228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1328-687A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909403 | |||||||
chr3:44909682 | C | G | 194 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(191): Show |
213 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.1328-408C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909682 | |||||||
chr3:44909911 | G | A | 78 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(75): Show |
86 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1328-179G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909911 | |||||||
chr3:44909942 | A | G | 193 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1328-148A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909942 | |||||||
chr3:44910439 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1606+71T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910439 | |||||||
chr3:44910473 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0175 |
3 | NA18952.hp2 NA19001.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1606+105G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910473 | |||||||
chr3:44910551 | A | G | 209 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(206): Show |
228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1606+183A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910551 | |||||||
chr3:44910574 | G | A | 78 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(75): Show |
86 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1606+206G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910574 | |||||||
chr3:44910698 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1607-260A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910698 | |||||||
chr3:44910768 | T | C | 6 | a0010c0008t0004g0149 a0010c0008t0004g0154 a0010c0008t0004g0157 others(3): Show |
6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1607-190T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910768 | |||||||
chr3:44910813 | T | C | 2 | a0003c0003t0001g0072 a0003c0003t0001g0074 |
2 | HG04199.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1607-145T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910813 | |||||||
chr3:44910915 | G | C | 199 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(196): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1607-43G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910915 | |||||||
chr3:44911165 | T | A | 1 | a0008c0006t0003g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1776+38T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 12/13 | chr3 | 44911165 | |||||||
chr3:44911188 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1776+61C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 12/13 | chr3 | 44911188 | |||||||
chr3:44911446 | A | G | 9 | a0002c0013t0001g0153 a0002c0013t0001g0155 a0002c0013t0001g0165 others(6): Show |
9 | HG02055.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1913+40A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911446 | |||||||
chr3:44911450 | A | C | 200 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(197): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1913+44A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911450 | |||||||
chr3:44911548 | G | T | 3 | a0002c0013t0001g0153 a0002c0013t0001g0155 a0002c0013t0001g0165 |
3 | HG02486.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1913+142G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911548 | |||||||
chr3:44911643 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1913+237G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911643 | |||||||
chr3:44911834 | C | T | 209 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(206): Show |
228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1913+428C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911834 | |||||||
chr3:44912006 | T | C | 1 | a0002c0002t0007g0263 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1913+600T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912006 | |||||||
chr3:44912010 | T | C | 1 | a0018c0028t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1913+604T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912010 | |||||||
chr3:44912034 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1913+628T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912034 | |||||||
chr3:44912245 | C | T | 3 | a0011c0011t0001g0037 a0011c0011t0001g0038 a0011c0011t0001g0039 |
3 | HG02809.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1913+839C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912245 | |||||||
chr3:44912429 | G | T | 1 | a0004c0004t0001g0235 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1913+1023G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912429 | |||||||
chr3:44912482 | A | G | 78 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(75): Show |
86 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1913+1076A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912482 | |||||||
chr3:44912548 | T | C | 4 | a0002c0013t0001g0153 a0002c0013t0001g0155 a0002c0013t0001g0165 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914-1036T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912548 | |||||||
chr3:44912710 | T | C | 4 | a0002c0013t0001g0153 a0002c0013t0001g0155 a0002c0013t0001g0165 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914-874T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912710 | |||||||
chr3:44912798 | C | T | 6 | a0011c0011t0001g0033 a0011c0011t0001g0035 a0011c0011t0001g0037 others(3): Show |
6 | HG02055.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1914-786C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912798 | |||||||
chr3:44912894 | T | C | 1 | a0002c0018t0002g0006 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1914-690T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912894 | |||||||
chr3:44912923 | T | A | 10 | a0006c0010t0003g0007 a0006c0010t0003g0047 a0006c0010t0003g0065 others(7): Show |
12 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1914-661T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912923 | |||||||
chr3:44912986 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0230 |
3 | HG00733.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1914-598C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912986 | |||||||
chr3:44912989 | A | G | 193 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1914-595A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912989 | |||||||
chr3:44913017 | A | G | 10 | a0002c0013t0001g0153 a0002c0013t0001g0155 a0002c0013t0001g0165 others(7): Show |
10 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1914-567A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44913017 | |||||||
chr3:44913065 | G | A | 2 | a0001c0014t0001g0024 a0001c0014t0001g0219 |
3 | HG02071.hp1 HG02129.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1914-519G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44913065 | |||||||
chr3:44913152 | A | G | 4 | a0002c0013t0001g0153 a0002c0013t0001g0155 a0002c0013t0001g0165 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914-432A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44913152 | |||||||
chr3:44913564 | T | C | 4 | a0002c0013t0001g0153 a0002c0013t0001g0155 a0002c0013t0001g0165 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914-20T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44913564 |