Item | Value |
---|---|
geneid | 7052 |
ensemblid | ENSG00000198959.12 |
hgncid | 11778 |
symbol | TGM2 |
name | transglutaminase 2 |
refseq_nuc | NM_004613.4 |
refseq_prot | NP_004604.2 |
ensembl_nuc | ENST00000361475.7 |
ensembl_prot | ENSP00000355330.2 |
mane_status | MANE Select |
chr | chr20 |
start | 38127385 |
end | 38165270 |
strand | - |
ver | v1.2 |
region | chr20:38127385-38165270 |
region5000 | chr20:38122385-38170270 |
regionname0 | TGM2_chr20_38127385_38165270 |
regionname5000 | TGM2_chr20_38122385_38170270 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 687 | 340 | 92 | 61 | 134 | 16 | 35 | 106 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0002 | 0/0 | 687 | 6 | 0 | 1 | 5 | 0 | 0 | 4 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0003 | 0/0 | 687 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0004 | 0/0 | 687 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0005 | 0/0 | 687 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0006 | 0/0 | 687 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0007 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0008 | 0/0 | 687 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0009 | 0/0 | 687 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0010 | 0/0 | 687 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0011 | 0/0 | 687 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0012 | 0/0 | 687 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
a0013 | 0/0 | 687 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | MAEEL others(682): Show |
chr20 | 38122385 | 38170270 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2061 | 201 | 47 | 45 | 68 | 13 | 26 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0002 | 0/0 | 2061 | 75 | 22 | 9 | 37 | 2 | 5 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0003 | 0/0 | 2061 | 21 | 0 | 0 | 21 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0004 | 0/0 | 2061 | 20 | 11 | 3 | 6 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0006 | 0/0 | 2061 | 5 | 5 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0007 | 0/0 | 2061 | 4 | 0 | 3 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0008 | 0/0 | 2061 | 3 | 3 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0009 | 0/0 | 2061 | 2 | 1 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0011 | 0/0 | 2061 | 2 | 0 | 0 | 0 | 0 | 2 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0016 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0022 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0024 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0025 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0026 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0027 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0001c0028 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0002c0005 | 0/0 | 2061 | 6 | 0 | 1 | 5 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0003c0012 | 0/0 | 2061 | 2 | 1 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0004c0013 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0005c0010 | 0/0 | 2061 | 2 | 0 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0006c0020 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0007c0019 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0008c0021 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0009c0014 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0010c0017 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0011c0023 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0012c0015 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 | ||
a0013c0018 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | ATGGC others(2056): Show |
chr20 | 38122385 | 38170270 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4970 | 155 | 30 | 42 | 49 | 12 | 20 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0001t0002 | 0/0 | 4970 | 3 | 1 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0001t0003 | 0/0 | 4975 | 21 | 0 | 0 | 17 | 0 | 4 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4970): Show |
chr20 | 38122385 | 38170270 |
a0001c0001t0004 | 0/0 | 4970 | 2 | 1 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0001t0005 | 0/0 | 4970 | 13 | 10 | 3 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0001t0009 | 0/0 | 4970 | 3 | 1 | 0 | 0 | 1 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0001t0011 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0001t0012 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0001t0013 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0001t0019 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0002t0001 | 0/0 | 4970 | 3 | 0 | 0 | 2 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0002t0002 | 0/0 | 4970 | 57 | 11 | 9 | 32 | 2 | 3 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0002t0006 | 0/0 | 4970 | 9 | 9 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0002t0011 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0002t0014 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0002t0015 | 0/0 | 4970 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0002t0016 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0002t0017 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0002t0018 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0003t0002 | 0/0 | 4970 | 20 | 0 | 0 | 20 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0003t0003 | 0/0 | 4975 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4970): Show |
chr20 | 38122385 | 38170270 |
a0001c0004t0004 | 0/0 | 4970 | 16 | 8 | 2 | 6 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0004t0010 | 0/0 | 4970 | 3 | 3 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0004t0021 | 0/0 | 4970 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0006t0007 | 0/0 | 4970 | 5 | 5 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0007t0002 | 0/0 | 4970 | 4 | 0 | 3 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0008t0008 | 0/0 | 4970 | 3 | 3 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0009t0007 | 0/0 | 4970 | 2 | 1 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0011t0001 | 0/0 | 4970 | 2 | 0 | 0 | 0 | 0 | 2 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0016t0001 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0022t0001 | 0/0 | 4970 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0024t0001 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0025t0004 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0026t0002 | 0/0 | 4970 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0027t0001 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0001c0028t0002 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0002c0005t0001 | 0/0 | 4970 | 6 | 0 | 1 | 5 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0003c0012t0002 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0003c0012t0020 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0004c0013t0005 | 0/0 | 4970 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0005c0010t0002 | 0/0 | 4970 | 2 | 0 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0006c0020t0002 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0007c0019t0002 | 0/0 | 4970 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0008c0021t0003 | 0/0 | 4975 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4970): Show |
chr20 | 38122385 | 38170270 |
a0009c0014t0003 | 0/0 | 4975 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4970): Show |
chr20 | 38122385 | 38170270 |
a0010c0017t0001 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0011c0023t0001 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0012c0015t0002 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
a0013c0018t0001 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | AGTGC others(4965): Show |
chr20 | 38122385 | 38170270 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 5 | 1 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0002 | 0/1 | 6 | 1 | 4 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0003 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0022 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0009g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0009g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0013g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0001t0019g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0014 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0006g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0006g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0014g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0015g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0016g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0017g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0002t0018g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0010g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0010g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0004t0021g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0006t0007g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0006t0007g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0006t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0007t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0007t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0007t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0007t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0008t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0008t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0008t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0009t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0009t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0011t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0016t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0022t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0024t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0025t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0026t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0027t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0001c0028t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0002c0005t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0002c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0002c0005t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0002c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0002c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0003c0012t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0003c0012t0020g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0004c0013t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0005c0010t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0005c0010t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0006c0020t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0007c0019t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0008c0021t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0009c0014t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0010c0017t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0011c0023t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0012c0015t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
a0013c0018t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00140 | hp1 | a0001 | c0022 | t0001 | g0177 | EUR | GBR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | GBR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0014 | EUR | FIN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0014 | EUR | FIN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00609 | hp2 | a0003 | c0012 | t0002 | g0227 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00621 | hp1 | a0002 | c0005 | t0001 | g0207 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0250 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00642 | hp2 | a0001 | c0004 | t0004 | g0274 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0244 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01109 | hp1 | a0001 | c0004 | t0004 | g0168 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01167 | hp1 | a0001 | c0009 | t0007 | g0146 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01175 | hp2 | a0001 | c0007 | t0002 | g0269 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01192 | hp2 | a0001 | c0007 | t0002 | g0070 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0163 | AMR | PUR | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01261 | hp1 | a0001 | c0004 | t0021 | g0301 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0197 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0238 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0292 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01993 | hp1 | a0002 | c0005 | t0001 | g0208 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02055 | hp1 | a0001 | c0004 | t0004 | g0149 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02056 | hp1 | a0006 | c0020 | t0002 | g0069 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02145 | hp2 | a0001 | c0001 | t0011 | g0128 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02257 | hp2 | a0001 | c0001 | t0013 | g0131 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0286 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02280 | hp1 | a0001 | c0002 | t0006 | g0010 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0064 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0272 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02451 | hp1 | a0001 | c0002 | t0014 | g0060 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02451 | hp2 | a0001 | c0002 | t0006 | g0023 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02572 | hp1 | a0001 | c0008 | t0008 | g0123 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02622 | hp1 | a0001 | c0004 | t0004 | g0135 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02622 | hp2 | a0001 | c0002 | t0006 | g0137 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02630 | hp2 | a0001 | c0002 | t0006 | g0158 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02647 | hp1 | a0004 | c0013 | t0005 | g0024 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02717 | hp1 | a0001 | c0004 | t0010 | g0297 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0159 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02809 | hp2 | a0001 | c0006 | t0007 | g0034 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02818 | hp1 | a0004 | c0013 | t0005 | g0024 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02886 | hp1 | a0007 | c0019 | t0002 | g0050 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02895 | hp1 | a0001 | c0002 | t0006 | g0141 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02895 | hp2 | a0001 | c0004 | t0010 | g0036 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02897 | hp1 | a0001 | c0004 | t0010 | g0036 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0100 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02965 | hp2 | a0001 | c0004 | t0004 | g0035 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02970 | hp2 | a0001 | c0008 | t0008 | g0129 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0294 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0255 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03098 | hp1 | a0001 | c0004 | t0004 | g0275 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03098 | hp2 | a0001 | c0002 | t0006 | g0023 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03139 | hp1 | a0001 | c0004 | t0004 | g0035 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03195 | hp1 | a0001 | c0002 | t0006 | g0010 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03195 | hp2 | a0001 | c0006 | t0007 | g0033 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03209 | hp2 | a0001 | c0002 | t0006 | g0010 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03453 | hp1 | a0001 | c0009 | t0007 | g0277 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03453 | hp2 | a0001 | c0004 | t0004 | g0293 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03486 | hp2 | a0001 | c0006 | t0007 | g0034 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0298 | AFR | ESN | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03540 | hp1 | a0001 | c0006 | t0007 | g0033 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03540 | hp2 | a0001 | c0025 | t0004 | g0130 | AFR | GWD | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03579 | hp1 | a0001 | c0004 | t0004 | g0187 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03579 | hp2 | a0003 | c0012 | t0020 | g0300 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0102 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03669 | hp2 | a0001 | c0011 | t0001 | g0019 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0290 | SAS | STU | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03831 | hp1 | a0001 | c0002 | t0015 | g0116 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03831 | hp2 | a0001 | c0011 | t0001 | g0019 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03834 | hp2 | a0001 | c0026 | t0002 | g0186 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0196 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0203 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03942 | hp2 | a0008 | c0021 | t0003 | g0098 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0265 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG04204 | hp2 | a0001 | c0007 | t0002 | g0271 | SAS | STU | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0258 | SAS | STU | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18522 | hp1 | a0001 | c0006 | t0007 | g0279 | AFR | YRI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | CHB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18612 | hp2 | a0009 | c0014 | t0003 | g0184 | EAS | CHB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18906 | hp1 | a0001 | c0004 | t0004 | g0169 | AFR | YRI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0150 | AFR | YRI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18952 | hp2 | a0001 | c0003 | t0003 | g0179 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18954 | hp1 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18962 | hp2 | a0001 | c0003 | t0002 | g0026 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18964 | hp1 | a0010 | c0017 | t0001 | g0077 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18964 | hp2 | a0001 | c0003 | t0002 | g0045 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18966 | hp1 | a0001 | c0003 | t0002 | g0044 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18966 | hp2 | a0001 | c0004 | t0004 | g0192 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18968 | hp1 | a0002 | c0005 | t0001 | g0027 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18971 | hp1 | a0001 | c0003 | t0002 | g0198 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18973 | hp2 | a0001 | c0003 | t0002 | g0199 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18974 | hp1 | a0001 | c0003 | t0002 | g0182 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18977 | hp1 | a0001 | c0004 | t0004 | g0140 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18977 | hp2 | a0001 | c0002 | t0017 | g0205 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18980 | hp1 | a0001 | c0003 | t0002 | g0195 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18983 | hp1 | a0001 | c0002 | t0016 | g0282 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18985 | hp2 | a0001 | c0003 | t0002 | g0201 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18987 | hp1 | a0001 | c0003 | t0002 | g0183 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18988 | hp1 | a0001 | c0003 | t0002 | g0218 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18991 | hp1 | a0001 | c0003 | t0002 | g0231 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18992 | hp1 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18994 | hp1 | a0001 | c0003 | t0002 | g0194 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18995 | hp2 | a0001 | c0003 | t0002 | g0026 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18999 | hp2 | a0011 | c0023 | t0001 | g0049 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19000 | hp1 | a0001 | c0004 | t0004 | g0236 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19000 | hp2 | a0005 | c0010 | t0002 | g0257 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19001 | hp1 | a0012 | c0015 | t0002 | g0185 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19001 | hp2 | a0013 | c0018 | t0001 | g0056 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19004 | hp2 | a0001 | c0002 | t0018 | g0065 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19007 | hp2 | a0001 | c0003 | t0002 | g0012 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19011 | hp1 | a0001 | c0004 | t0004 | g0007 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19012 | hp2 | a0002 | c0005 | t0001 | g0209 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | LWK | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0296 | AFR | LWK | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0037 | AFR | LWK | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19057 | hp1 | a0001 | c0028 | t0002 | g0112 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19065 | hp1 | a0001 | c0003 | t0002 | g0012 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19068 | hp1 | a0001 | c0004 | t0004 | g0007 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19068 | hp2 | a0002 | c0005 | t0001 | g0027 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19080 | hp1 | a0005 | c0010 | t0002 | g0268 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19082 | hp2 | a0001 | c0004 | t0004 | g0007 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19084 | hp2 | a0002 | c0005 | t0001 | g0210 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19085 | hp1 | a0001 | c0003 | t0002 | g0012 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19086 | hp1 | a0001 | c0003 | t0002 | g0202 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19089 | hp2 | a0001 | c0016 | t0001 | g0073 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0171 | AFR | YRI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | YRI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA20752 | hp1 | a0001 | c0001 | t0009 | g0299 | EUR | TSI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0085 | SAS | GIH | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA20905 | hp2 | a0001 | c0001 | t0009 | g0295 | SAS | GIH | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG01123 | hp2 | a0001 | c0007 | t0002 | g0270 | AMR | CLM | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02559 | hp1 | a0001 | c0027 | t0001 | g0170 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03471 | hp1 | a0001 | c0024 | t0001 | g0136 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG03471 | hp2 | a0001 | c0008 | t0008 | g0154 | AFR | MSL | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0276 | AFR | USA | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0101 | AFR | USA | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA21309 | hp1 | a0001 | c0002 | t0011 | g0126 | AFR | LWK | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0002 | REF | REF | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0022 | REF | REF | TGM2_chr20_38122385_38170270 | TGM2 | chr20 | 38122385 | 38170270 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38132492 | C | A | 1 | a0003 | 2 | HG00609.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.1624G>T | p.Val542Phe | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/13 | 1696/4970 | 1624/2064 | 542/687 | chr20 | 38132492 | |||
chr20:38138122 | G | A | 1 | a0011 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.1606C>T | p.Pro536Ser | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/13 | 1678/4970 | 1606/2064 | 536/687 | chr20 | 38138122 | |||
chr20:38138161 | C | T | 1 | a0008 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1567G>A | p.Glu523Lys | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/13 | 1639/4970 | 1567/2064 | 523/687 | chr20 | 38138161 | |||
chr20:38138322 | T | C | 1 | a0006 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1406A>G | p.Glu469Gly | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/13 | 1478/4970 | 1406/2064 | 469/687 | chr20 | 38138322 | |||
chr20:38139448 | G | A | 1 | a0004 | 2 | HG02647.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.1306C>T | p.Arg436Trp | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/13 | 1378/4970 | 1306/2064 | 436/687 | chr20 | 38139448 | |||
chr20:38139463 | C | A | 1 | a0005 | 2 | NA19000.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.1291G>T | p.Val431Leu | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/13 | 1363/4970 | 1291/2064 | 431/687 | chr20 | 38139463 | |||
chr20:38139624 | C | T | 1 | a0007 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1130G>A | p.Arg377His | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/13 | 1202/4970 | 1130/2064 | 377/687 | chr20 | 38139624 | |||
chr20:38146778 | G | T | 1 | a0013 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.798C>A | p.Asn266Lys | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/13 | 870/4970 | 798/2064 | 266/687 | chr20 | 38146778 | |||
chr20:38148001 | C | T | 1 | a0010 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.641G>A | p.Arg214His | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/13 | 713/4970 | 641/2064 | 214/687 | chr20 | 38148001 | |||
chr20:38156053 | C | T | 1 | a0002 | 6 | HG00621.hp1 HG01993.hp1 NA18968.hp1 others(3): Show |
missense_variant | MODERATE | c.227G>A | p.Arg76His | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/13 | 299/4970 | 227/2064 | 76/687 | chr20 | 38156053 | |||
chr20:38161426 | C | T | 1 | a0012 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.184G>A | p.Val62Met | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/13 | 256/4970 | 184/2064 | 62/687 | chr20 | 38161426 | |||
chr20:38161467 | C | T | 1 | a0009 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.143G>A | p.Arg48His | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/13 | 215/4970 | 143/2064 | 48/687 | chr20 | 38161467 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38130360 | G | A | 2 | a0001c0006 a0001c0009 |
7 | HG01167.hp1 HG02809.hp2 HG03195.hp2 others(4): Show |
synonymous_variant | LOW | c.1923C>T | p.Pro641Pro | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 1995/4970 | 1923/2064 | 641/687 | chr20 | 38130360 | |||
chr20:38131119 | C | T | 3 | a0001c0003 a0003c0012 a0012c0015 |
24 | HG00609.hp2 HG03579.hp2 NA18945.hp2 others(21): Show |
synonymous_variant | LOW | c.1887G>A | p.Leu629Leu | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/13 | 1959/4970 | 1887/2064 | 629/687 | chr20 | 38131119 | |||
chr20:38132484 | A | G | 1 | a0001c0022 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.1632T>C | p.Leu544Leu | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/13 | 1704/4970 | 1632/2064 | 544/687 | chr20 | 38132484 | |||
chr20:38139584 | C | T | 1 | a0001c0007 | 4 | HG01123.hp2 HG01175.hp2 HG01192.hp2 others(1): Show |
synonymous_variant | LOW | c.1170G>A | p.Ala390Ala | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/13 | 1242/4970 | 1170/2064 | 390/687 | chr20 | 38139584 | |||
chr20:38142075 | G | A | 1 | a0001c0024 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.984C>T | p.Ser328Ser | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/13 | 1056/4970 | 984/2064 | 328/687 | chr20 | 38142075 | |||
chr20:38142081 | G | A | 1 | a0001c0008 | 3 | HG02572.hp1 HG02970.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.978C>T | p.Asp326Asp | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/13 | 1050/4970 | 978/2064 | 326/687 | chr20 | 38142081 | |||
chr20:38142117 | C | T | 1 | a0001c0011 | 2 | HG03669.hp2 HG03831.hp2 |
synonymous_variant | LOW | c.942G>A | p.Glu314Glu | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/13 | 1014/4970 | 942/2064 | 314/687 | chr20 | 38142117 | |||
chr20:38142186 | C | T | 9 | a0001c0002 a0001c0006 a0001c0007 others(6): Show |
92 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(89): Show |
synonymous_variant | LOW | c.873G>A | p.Leu291Leu | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/13 | 945/4970 | 873/2064 | 291/687 | chr20 | 38142186 | |||
chr20:38146730 | G | A | 1 | a0001c0025 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.846C>T | p.Ala282Ala | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/13 | 918/4970 | 846/2064 | 282/687 | chr20 | 38146730 | |||
chr20:38146733 | G | A | 1 | a0001c0004 | 20 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
synonymous_variant | LOW | c.843C>T | p.Ala281Ala | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/13 | 915/4970 | 843/2064 | 281/687 | chr20 | 38146733 | |||
chr20:38146841 | G | A | 1 | a0001c0026 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.735C>T | p.Tyr245Tyr | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/13 | 807/4970 | 735/2064 | 245/687 | chr20 | 38146841 | |||
chr20:38147991 | G | C | 1 | a0001c0006 | 5 | HG02809.hp2 HG03195.hp2 HG03486.hp2 others(2): Show |
synonymous_variant | LOW | c.651C>G | p.Pro217Pro | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/13 | 723/4970 | 651/2064 | 217/687 | chr20 | 38147991 | |||
chr20:38151035 | C | T | 1 | a0001c0016 | 1 | NA19089.hp2 | synonymous_variant | LOW | c.456G>A | p.Ser152Ser | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/13 | 528/4970 | 456/2064 | 152/687 | chr20 | 38151035 | |||
chr20:38155860 | G | A | 1 | a0001c0027 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.420C>T | p.Asn140Asn | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/13 | 492/4970 | 420/2064 | 140/687 | chr20 | 38155860 | |||
chr20:38156067 | G | A | 1 | a0001c0028 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.213C>T | p.Ala71Ala | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/13 | 285/4970 | 213/2064 | 71/687 | chr20 | 38156067 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38127439 | T | C | 1 | a0001c0002t0006 | 9 | HG02280.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2780A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2780 | chr20 | 38127439 | ||||||
chr20:38127530 | G | C | 20 | a0001c0001t0002 a0001c0001t0012 a0001c0002t0002 others(17): Show |
108 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2689C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2689 | chr20 | 38127530 | ||||||
chr20:38127575 | T | A | 1 | a0001c0002t0017 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2644A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2644 | chr20 | 38127575 | ||||||
chr20:38127576 | C | T | 1 | a0001c0002t0017 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2643G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2643 | chr20 | 38127576 | ||||||
chr20:38127600 | G | A | 2 | a0001c0006t0007 a0001c0009t0007 |
7 | HG01167.hp1 HG02809.hp2 HG03195.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2619C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2619 | chr20 | 38127600 | ||||||
chr20:38127958 | C | T | 2 | a0001c0001t0005 a0004c0013t0005 |
15 | HG00741.hp2 HG01243.hp2 HG01361.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2261G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2261 | chr20 | 38127958 | ||||||
chr20:38127973 | G | A | 1 | a0001c0002t0014 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2246C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2246 | chr20 | 38127973 | ||||||
chr20:38127998 | G | C | 2 | a0001c0001t0005 a0004c0013t0005 |
15 | HG00741.hp2 HG01243.hp2 HG01361.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2221C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2221 | chr20 | 38127998 | ||||||
chr20:38128112 | T | A | 5 | a0001c0001t0004 a0001c0004t0004 a0001c0004t0010 others(2): Show |
23 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2107A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2107 | chr20 | 38128112 | ||||||
chr20:38128151 | G | T | 1 | a0001c0002t0017 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2068C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2068 | chr20 | 38128151 | ||||||
chr20:38128152 | C | G | 1 | a0001c0002t0017 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2067G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2067 | chr20 | 38128152 | ||||||
chr20:38128198 | C | T | 2 | a0001c0001t0013 a0001c0001t0019 |
2 | HG02257.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2021G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 2021 | chr20 | 38128198 | ||||||
chr20:38128446 | A | ACAGAC | 4 | a0001c0001t0003 a0001c0003t0003 a0008c0021t0003 others(1): Show |
24 | HG00621.hp2 HG02056.hp2 HG02080.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1768_*1772dupGTCT others(1): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 1772 | chr20 | 38128446 | ||||||
chr20:38128466 | G | A | 1 | a0001c0002t0015 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1753C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 1753 | chr20 | 38128466 | ||||||
chr20:38128533 | G | A | 1 | a0001c0002t0016 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 1686 | chr20 | 38128533 | ||||||
chr20:38128851 | G | C | 1 | a0001c0002t0017 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1368C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 1368 | chr20 | 38128851 | ||||||
chr20:38129260 | G | C | 1 | a0001c0008t0008 | 3 | HG02572.hp1 HG02970.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*959C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 959 | chr20 | 38129260 | ||||||
chr20:38129373 | A | G | 2 | a0001c0006t0007 a0001c0009t0007 |
7 | HG01167.hp1 HG02809.hp2 HG03195.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*846T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 846 | chr20 | 38129373 | ||||||
chr20:38129560 | G | A | 1 | a0001c0002t0018 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 659 | chr20 | 38129560 | ||||||
chr20:38129644 | G | A | 5 | a0001c0001t0004 a0001c0004t0004 a0001c0004t0010 others(2): Show |
23 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*575C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 575 | chr20 | 38129644 | ||||||
chr20:38129768 | G | A | 5 | a0001c0001t0004 a0001c0004t0004 a0001c0004t0010 others(2): Show |
23 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 451 | chr20 | 38129768 | ||||||
chr20:38129973 | A | G | 1 | a0001c0008t0008 | 3 | HG02572.hp1 HG02970.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*246T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 246 | chr20 | 38129973 | ||||||
chr20:38130139 | G | A | 2 | a0001c0001t0011 a0001c0002t0011 |
2 | HG02145.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*80C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 13/13 | 80 | chr20 | 38130139 | ||||||
chr20:38165206 | C | T | 1 | a0001c0001t0012 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/13 | 8 | chr20 | 38165206 | ||||||
chr20:38165209 | G | A | 1 | a0003c0012t0020 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/13 | 11 | chr20 | 38165209 | ||||||
chr20:38165232 | G | A | 4 | a0001c0001t0009 a0001c0001t0019 a0001c0004t0010 others(1): Show |
8 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/13 | chr20 | 38165232 | |||||||
chr20:38165240 | C | A | 1 | a0001c0004t0021 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/13 | 42 | chr20 | 38165240 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38130376 | G | C | 111 | a0001c0001t0001g0132 a0001c0001t0002g0052 a0001c0001t0002g0162 others(108): Show |
121 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(118): Show |
splice_region_variant&intron_variant | LOW | c.1914-7C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130376 | |||||||
chr20:38130383 | G | A | 12 | a0001c0001t0005g0041 a0001c0001t0005g0120 a0001c0001t0005g0121 others(9): Show |
13 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1914-14C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130383 | |||||||
chr20:38130384 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1914-15C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130384 | |||||||
chr20:38130430 | G | A | 2 | a0001c0001t0001g0132 a0001c0027t0001g0170 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1914-61C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130430 | |||||||
chr20:38130456 | C | T | 79 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0155 others(76): Show |
83 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1914-87G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130456 | |||||||
chr20:38130553 | G | A | 1 | a0001c0002t0006g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1914-184C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130553 | |||||||
chr20:38130625 | T | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0232 |
2 | HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1914-256A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130625 | |||||||
chr20:38130705 | AAAG | A | 19 | a0001c0001t0004g0193 a0001c0001t0004g0196 a0001c0004t0004g0007 others(16): Show |
23 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1914-339_1914-337d others(5): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130705 | |||||||
chr20:38130779 | G | T | 2 | a0001c0002t0002g0124 a0001c0002t0002g0127 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1913+314C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130779 | |||||||
chr20:38130972 | C | CTG | 19 | a0001c0001t0004g0193 a0001c0001t0004g0196 a0001c0004t0004g0007 others(16): Show |
23 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1913+119_1913+120d others(4): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38130972 | |||||||
chr20:38131003 | G | A | 12 | a0001c0001t0005g0041 a0001c0001t0005g0120 a0001c0001t0005g0121 others(9): Show |
13 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1913+90C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 12/12 | chr20 | 38131003 | |||||||
chr20:38131289 | A | C | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1777-60T>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38131289 | |||||||
chr20:38131349 | A | AC | 114 | a0001c0001t0002g0052 a0001c0001t0002g0162 a0001c0001t0005g0041 others(111): Show |
127 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1777-121dupG | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38131349 | |||||||
chr20:38131555 | A | G | 7 | a0001c0002t0006g0010 a0001c0002t0006g0023 a0001c0002t0006g0137 others(4): Show |
10 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1777-326T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38131555 | |||||||
chr20:38131844 | C | G | 2 | a0001c0001t0005g0121 a0001c0001t0005g0142 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1776+496G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38131844 | |||||||
chr20:38132067 | G | A | 1 | a0001c0027t0001g0170 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1776+273C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38132067 | |||||||
chr20:38132157 | G | A | 102 | a0001c0001t0002g0052 a0001c0001t0005g0134 a0001c0001t0005g0163 others(99): Show |
114 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1776+183C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38132157 | |||||||
chr20:38132166 | A | G | 102 | a0001c0001t0002g0052 a0001c0001t0005g0134 a0001c0001t0005g0163 others(99): Show |
114 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1776+174T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38132166 | |||||||
chr20:38132196 | A | G | 102 | a0001c0001t0002g0052 a0001c0001t0005g0134 a0001c0001t0005g0163 others(99): Show |
114 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1776+144T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38132196 | |||||||
chr20:38132271 | G | T | 1 | a0001c0001t0001g0013 | 3 | HG01069.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1776+69C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38132271 | |||||||
chr20:38132309 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0232 |
2 | HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1776+31C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 11/12 | chr20 | 38132309 | |||||||
chr20:38132593 | G | A | 26 | a0001c0001t0005g0134 a0001c0001t0005g0163 a0001c0003t0002g0012 others(23): Show |
32 | HG00609.hp2 HG01167.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1616-93C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38132593 | |||||||
chr20:38132612 | G | A | 69 | a0001c0001t0002g0052 a0001c0002t0002g0014 a0001c0002t0002g0031 others(66): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1616-112C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38132612 | |||||||
chr20:38132655 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0053 others(9): Show |
16 | HG00642.hp1 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1616-155G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38132655 | |||||||
chr20:38132697 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1616-197C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38132697 | |||||||
chr20:38132707 | C | T | 1 | a0001c0002t0011g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1616-207G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38132707 | |||||||
chr20:38132800 | G | A | 69 | a0001c0001t0002g0052 a0001c0002t0002g0014 a0001c0002t0002g0031 others(66): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1616-300C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38132800 | |||||||
chr20:38132800 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1616-300C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38132800 | |||||||
chr20:38132834 | G | C | 2 | a0001c0001t0011g0128 a0001c0002t0011g0126 |
2 | HG02145.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1616-334C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38132834 | |||||||
chr20:38132991 | A | G | 1 | a0001c0002t0002g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1616-491T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38132991 | |||||||
chr20:38133103 | T | C | 1 | a0001c0002t0018g0065 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1616-603A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38133103 | |||||||
chr20:38133240 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1616-740T>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38133240 | |||||||
chr20:38133415 | G | A | 2 | a0001c0001t0011g0128 a0001c0002t0011g0126 |
2 | HG02145.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1616-915C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38133415 | |||||||
chr20:38133417 | T | C | 1 | a0001c0001t0003g0062 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1616-917A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38133417 | |||||||
chr20:38133492 | G | A | 5 | a0001c0006t0007g0033 a0001c0006t0007g0034 a0001c0006t0007g0279 others(2): Show |
7 | HG01167.hp1 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1616-992C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38133492 | |||||||
chr20:38133693 | C | T | 18 | a0001c0003t0002g0012 a0001c0003t0002g0025 a0001c0003t0002g0026 others(15): Show |
22 | HG00609.hp2 HG03579.hp2 NA18945.hp2 others(19): Show |
intron_variant | MODIFIER | c.1616-1193G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38133693 | |||||||
chr20:38133751 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1616-1251G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38133751 | |||||||
chr20:38133839 | C | T | 7 | a0001c0002t0002g0031 a0001c0002t0002g0173 a0001c0002t0002g0237 others(4): Show |
8 | NA18944.hp1 NA18981.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1616-1339G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38133839 | |||||||
chr20:38134030 | C | T | 1 | a0001c0003t0002g0199 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1616-1530G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38134030 | |||||||
chr20:38134151 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0155 others(1): Show |
5 | HG02486.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1616-1651A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38134151 | |||||||
chr20:38134175 | C | G | 76 | a0001c0001t0002g0052 a0001c0002t0002g0014 a0001c0002t0002g0031 others(73): Show |
82 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1616-1675G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38134175 | |||||||
chr20:38134653 | G | C | 77 | a0001c0001t0002g0052 a0001c0002t0002g0014 a0001c0002t0002g0031 others(74): Show |
83 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1616-2153C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38134653 | |||||||
chr20:38134792 | A | G | 129 | a0001c0001t0001g0084 a0001c0001t0001g0133 a0001c0001t0002g0052 others(126): Show |
145 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1616-2292T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38134792 | |||||||
chr20:38134896 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0086 others(1): Show |
4 | NA18984.hp2 NA19007.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1616-2396C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38134896 | |||||||
chr20:38134964 | G | A | 77 | a0001c0001t0002g0052 a0001c0002t0002g0014 a0001c0002t0002g0031 others(74): Show |
83 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1616-2464C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38134964 | |||||||
chr20:38135027 | A | G | 108 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0133 others(105): Show |
121 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1616-2527T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135027 | |||||||
chr20:38135165 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1616-2665A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135165 | |||||||
chr20:38135264 | T | C | 8 | a0001c0002t0006g0010 a0001c0002t0006g0023 a0001c0002t0006g0137 others(5): Show |
11 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1616-2764A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135264 | |||||||
chr20:38135313 | G | A | 1 | a0001c0027t0001g0170 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1615+2800C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135313 | |||||||
chr20:38135404 | T | TAC | 13 | a0001c0001t0001g0021 a0001c0001t0001g0055 a0001c0001t0001g0071 others(10): Show |
14 | HG01884.hp2 HG01891.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1615+2707_1615+270 others(6): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | T | TACAC | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
87 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1615+2705_1615+270 others(8): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | T | TACACAC | 6 | a0001c0001t0001g0029 a0001c0001t0001g0176 a0001c0001t0001g0223 others(3): Show |
7 | HG01081.hp2 HG01192.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615+2703_1615+270 others(10): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | T | TACACACA others(1): Show |
5 | a0001c0001t0001g0224 a0001c0001t0001g0288 a0001c0002t0002g0294 others(2): Show |
5 | HG01433.hp1 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615+2701_1615+270 others(12): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | T | TACACACA others(5): Show |
10 | a0001c0002t0002g0102 a0001c0002t0002g0252 a0001c0002t0002g0256 others(7): Show |
12 | HG02280.hp1 HG02300.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1615+2697_1615+270 others(16): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | T | TACACACA others(7): Show |
19 | a0001c0002t0002g0100 a0001c0002t0002g0124 a0001c0002t0002g0127 others(16): Show |
20 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1615+2695_1615+270 others(18): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | T | TACACACA others(9): Show |
26 | a0001c0002t0002g0014 a0001c0002t0002g0039 a0001c0002t0002g0040 others(23): Show |
28 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.1615+2693_1615+270 others(20): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | T | TACACACA others(11): Show |
14 | a0001c0002t0002g0031 a0001c0002t0002g0103 a0001c0002t0002g0150 others(11): Show |
15 | HG02056.hp1 HG02083.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1615+2691_1615+270 others(22): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | T | TACACACA others(13): Show |
3 | a0001c0002t0002g0066 a0001c0002t0002g0068 a0001c0002t0002g0265 |
3 | HG02071.hp2 HG04184.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1615+2689_1615+270 others(24): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | TAC | T | 13 | a0001c0001t0005g0041 a0001c0001t0005g0120 a0001c0001t0005g0121 others(10): Show |
14 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1615+2707_1615+270 others(6): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135404 | TACAC | T | 6 | a0001c0001t0001g0109 a0001c0006t0007g0033 a0001c0006t0007g0034 others(3): Show |
8 | HG01167.hp1 HG02027.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615+2705_1615+270 others(8): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135404 | |||||||
chr20:38135434 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0095 a0001c0002t0002g0294 |
3 | HG02976.hp1 NA19004.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1615+2679A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135434 | |||||||
chr20:38135550 | CCAGGCAG | C | 128 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0125 others(125): Show |
145 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1615+2556_1615+256 others(11): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135550 | |||||||
chr20:38135692 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1615+2421C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135692 | |||||||
chr20:38135780 | G | A | 2 | a0001c0001t0005g0134 a0001c0001t0005g0163 |
2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1615+2333C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135780 | |||||||
chr20:38135840 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1615+2273C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135840 | |||||||
chr20:38135861 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1615+2252T>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38135861 | |||||||
chr20:38136136 | G | T | 1 | a0002c0005t0001g0027 | 2 | NA18968.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1615+1977C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136136 | |||||||
chr20:38136140 | C | A | 75 | a0001c0002t0002g0014 a0001c0002t0002g0031 a0001c0002t0002g0039 others(72): Show |
81 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1615+1973G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136140 | |||||||
chr20:38136221 | G | T | 2 | a0001c0002t0006g0010 a0001c0002t0006g0159 |
4 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615+1892C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136221 | |||||||
chr20:38136251 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0155 others(1): Show |
5 | HG02486.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615+1862C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136251 | |||||||
chr20:38136276 | G | A | 1 | a0001c0001t0011g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1615+1837C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136276 | |||||||
chr20:38136279 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0009g0295 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1615+1834A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136279 | |||||||
chr20:38136375 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1615+1738C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136375 | |||||||
chr20:38136386 | A | G | 1 | a0007c0019t0002g0050 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1615+1727T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136386 | |||||||
chr20:38136387 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1615+1726G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136387 | |||||||
chr20:38136702 | C | T | 75 | a0001c0002t0002g0014 a0001c0002t0002g0031 a0001c0002t0002g0039 others(72): Show |
81 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1615+1411G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136702 | |||||||
chr20:38136809 | T | C | 4 | a0001c0002t0002g0031 a0001c0002t0002g0173 a0001c0002t0002g0237 others(1): Show |
5 | NA18944.hp1 NA18981.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615+1304A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136809 | |||||||
chr20:38136819 | G | A | 1 | a0001c0002t0002g0255 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1615+1294C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136819 | |||||||
chr20:38136857 | T | A | 1 | a0001c0002t0002g0264 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1615+1256A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136857 | |||||||
chr20:38136990 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1615+1123G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38136990 | |||||||
chr20:38137003 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1615+1110G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137003 | |||||||
chr20:38137132 | C | T | 5 | a0001c0006t0007g0033 a0001c0006t0007g0034 a0001c0006t0007g0279 others(2): Show |
7 | HG01167.hp1 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615+981G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137132 | |||||||
chr20:38137199 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0089 a0001c0001t0001g0094 others(3): Show |
9 | HG00099.hp1 HG01361.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615+914A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137199 | |||||||
chr20:38137231 | T | C | 4 | a0001c0004t0004g0135 a0001c0004t0004g0168 a0001c0004t0004g0169 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615+882A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137231 | |||||||
chr20:38137348 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1615+765C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137348 | |||||||
chr20:38137358 | G | A | 12 | a0001c0001t0005g0041 a0001c0001t0005g0120 a0001c0001t0005g0121 others(9): Show |
13 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1615+755C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137358 | |||||||
chr20:38137436 | G | T | 1 | a0001c0002t0002g0241 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1615+677C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137436 | |||||||
chr20:38137501 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1615+612C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137501 | |||||||
chr20:38137573 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1615+540G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137573 | |||||||
chr20:38137617 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1615+496A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137617 | |||||||
chr20:38137827 | G | C | 1 | a0001c0003t0002g0218 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1615+286C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137827 | |||||||
chr20:38137830 | C | G | 1 | a0001c0003t0002g0218 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1615+283G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137830 | |||||||
chr20:38137849 | T | C | 1 | a0001c0001t0003g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1615+264A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137849 | |||||||
chr20:38137873 | C | T | 2 | a0001c0002t0002g0276 a0001c0002t0002g0286 |
2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1615+240G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137873 | |||||||
chr20:38137998 | G | A | 67 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0125 others(64): Show |
77 | HG00609.hp2 HG00642.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.1615+115C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 10/12 | chr20 | 38137998 | |||||||
chr20:38138393 | G | A | 1 | a0002c0005t0001g0208 | 1 | HG01993.hp1 | splice_region_variant&intron_variant | LOW | c.1343-8C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38138393 | |||||||
chr20:38138440 | G | C | 1 | a0001c0002t0002g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1343-55C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38138440 | |||||||
chr20:38138640 | G | T | 1 | a0001c0001t0003g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1343-255C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38138640 | |||||||
chr20:38138645 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1343-260A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38138645 | |||||||
chr20:38138701 | T | C | 68 | a0001c0002t0001g0067 a0001c0002t0002g0014 a0001c0002t0002g0031 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1343-316A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38138701 | |||||||
chr20:38138919 | C | G | 1 | a0001c0001t0012g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1342+493G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38138919 | |||||||
chr20:38139043 | T | A | 2 | a0001c0002t0006g0137 a0001c0002t0006g0141 |
2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1342+369A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38139043 | |||||||
chr20:38139287 | T | C | 1 | a0001c0002t0002g0266 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1342+125A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38139287 | |||||||
chr20:38139290 | G | T | 1 | a0007c0019t0002g0050 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1342+122C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38139290 | |||||||
chr20:38139328 | C | T | 1 | a0001c0002t0002g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1342+84G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38139328 | |||||||
chr20:38139329 | G | A | 1 | a0001c0001t0004g0193 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1342+83C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38139329 | |||||||
chr20:38139343 | G | A | 1 | a0001c0003t0002g0199 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1342+69C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 9/12 | chr20 | 38139343 | |||||||
chr20:38139662 | A | G | 46 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0125 others(43): Show |
55 | HG00609.hp2 HG00642.hp2 HG01109.hp1 others(52): Show |
splice_region_variant&intron_variant | LOW | c.1100-8T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38139662 | |||||||
chr20:38139856 | C | A | 19 | a0001c0001t0002g0162 a0001c0001t0004g0193 a0001c0001t0012g0037 others(16): Show |
23 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1100-202G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38139856 | |||||||
chr20:38139907 | C | T | 82 | a0001c0002t0001g0067 a0001c0002t0002g0014 a0001c0002t0002g0031 others(79): Show |
90 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1100-253G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38139907 | |||||||
chr20:38140119 | AGAGTGGA others(3): Show |
A | 1 | a0001c0001t0001g0200 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1100-475_1100-466d others(12): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140119 | |||||||
chr20:38140186 | T | C | 5 | a0001c0006t0007g0033 a0001c0006t0007g0034 a0001c0006t0007g0279 others(2): Show |
7 | HG01167.hp1 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1100-532A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140186 | |||||||
chr20:38140232 | C | T | 38 | a0001c0001t0001g0132 a0001c0001t0002g0162 a0001c0001t0004g0193 others(35): Show |
43 | HG00642.hp2 HG00741.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1100-578G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140232 | |||||||
chr20:38140272 | C | A | 68 | a0001c0002t0001g0067 a0001c0002t0002g0014 a0001c0002t0002g0031 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1100-618G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140272 | |||||||
chr20:38140354 | C | T | 19 | a0001c0001t0002g0162 a0001c0001t0004g0193 a0001c0001t0012g0037 others(16): Show |
23 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1100-700G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140354 | |||||||
chr20:38140415 | A | G | 25 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0125 others(22): Show |
30 | HG00609.hp2 HG02486.hp1 HG02572.hp2 others(27): Show |
intron_variant | MODIFIER | c.1100-761T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140415 | |||||||
chr20:38140426 | C | A | 1 | a0001c0002t0014g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1100-772G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140426 | |||||||
chr20:38140454 | G | A | 1 | a0001c0025t0004g0130 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1100-800C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140454 | |||||||
chr20:38140510 | C | T | 147 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0125 others(144): Show |
165 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1099+772G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140510 | |||||||
chr20:38140597 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1099+685G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140597 | |||||||
chr20:38140631 | G | A | 26 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0125 others(23): Show |
31 | HG00609.hp2 HG01891.hp2 HG02486.hp1 others(28): Show |
intron_variant | MODIFIER | c.1099+651C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140631 | |||||||
chr20:38140900 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1099+382T>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38140900 | |||||||
chr20:38141048 | A | AT | 5 | a0001c0001t0001g0003 a0001c0001t0001g0074 a0001c0001t0001g0079 others(2): Show |
8 | HG00642.hp1 HG00738.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099+233dupA | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38141048 | |||||||
chr20:38141084 | C | T | 83 | a0001c0002t0001g0061 a0001c0002t0001g0067 a0001c0002t0002g0014 others(80): Show |
91 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1099+198G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38141084 | |||||||
chr20:38141085 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0119 |
3 | HG00558.hp1 HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1099+197G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 8/12 | chr20 | 38141085 | |||||||
chr20:38141390 | G | A | 83 | a0001c0002t0001g0061 a0001c0002t0001g0067 a0001c0002t0001g0258 others(80): Show |
91 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(88): Show |
splice_region_variant&intron_variant | LOW | c.996-5C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141390 | |||||||
chr20:38141437 | G | A | 85 | a0001c0001t0001g0226 a0001c0001t0003g0203 a0001c0002t0001g0061 others(82): Show |
93 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.996-52C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141437 | |||||||
chr20:38141447 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.996-62T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141447 | |||||||
chr20:38141539 | C | G | 19 | a0001c0001t0002g0162 a0001c0001t0004g0193 a0001c0001t0012g0037 others(16): Show |
23 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.996-154G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141539 | |||||||
chr20:38141542 | G | A | 1 | a0008c0021t0003g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.996-157C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141542 | |||||||
chr20:38141640 | C | T | 12 | a0001c0001t0005g0041 a0001c0001t0005g0120 a0001c0001t0005g0121 others(9): Show |
13 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.996-255G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141640 | |||||||
chr20:38141717 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.996-332G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141717 | |||||||
chr20:38141792 | T | A | 1 | a0001c0002t0006g0159 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.995+272A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141792 | |||||||
chr20:38141848 | T | C | 1 | a0001c0002t0001g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.995+216A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141848 | |||||||
chr20:38141972 | C | T | 25 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0133 others(22): Show |
30 | HG00609.hp2 HG01891.hp2 HG02486.hp1 others(27): Show |
intron_variant | MODIFIER | c.995+92G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 7/12 | chr20 | 38141972 | |||||||
chr20:38142338 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0155 others(1): Show |
5 | HG02486.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-139C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38142338 | |||||||
chr20:38142391 | C | T | 1 | a0001c0002t0002g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.860-192G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38142391 | |||||||
chr20:38142541 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.860-342T>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38142541 | |||||||
chr20:38142641 | G | A | 20 | a0001c0001t0001g0132 a0001c0001t0005g0041 a0001c0001t0005g0120 others(17): Show |
21 | HG00741.hp2 HG01243.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.860-442C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38142641 | |||||||
chr20:38142976 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.860-777T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38142976 | |||||||
chr20:38143345 | C | A | 1 | a0008c0021t0003g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.860-1146G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143345 | |||||||
chr20:38143384 | C | T | 1 | a0001c0002t0002g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.860-1185G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143384 | |||||||
chr20:38143393 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0176 |
3 | HG01192.hp1 HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.860-1194C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143393 | |||||||
chr20:38143411 | C | G | 1 | a0003c0012t0020g0300 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.860-1212G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143411 | |||||||
chr20:38143412 | G | A | 1 | a0001c0002t0002g0256 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.860-1213C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143412 | |||||||
chr20:38143612 | C | T | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0214 others(1): Show |
4 | HG02080.hp1 HG02135.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-1413G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143612 | |||||||
chr20:38143618 | G | A | 1 | a0001c0002t0014g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.860-1419C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143618 | |||||||
chr20:38143728 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.860-1529A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143728 | |||||||
chr20:38143738 | G | A | 14 | a0001c0001t0002g0162 a0001c0001t0012g0037 a0001c0004t0004g0007 others(11): Show |
18 | HG00642.hp2 HG01261.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.860-1539C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143738 | |||||||
chr20:38143823 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.860-1624C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143823 | |||||||
chr20:38143848 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0079 |
2 | HG01934.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.860-1649G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143848 | |||||||
chr20:38143927 | C | G | 1 | a0001c0002t0002g0042 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.860-1728G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143927 | |||||||
chr20:38143928 | G | A | 1 | a0001c0001t0001g0006 | 3 | HG01070.hp1 HG01071.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.860-1729C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38143928 | |||||||
chr20:38144049 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.860-1850G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144049 | |||||||
chr20:38144090 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.860-1891G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144090 | |||||||
chr20:38144118 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0155 others(1): Show |
5 | HG02486.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-1919C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144118 | |||||||
chr20:38144197 | C | T | 21 | a0001c0001t0001g0133 a0001c0001t0004g0193 a0001c0003t0002g0012 others(18): Show |
25 | HG00609.hp2 HG02145.hp1 HG03579.hp2 others(22): Show |
intron_variant | MODIFIER | c.860-1998G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144197 | |||||||
chr20:38144240 | G | A | 1 | a0001c0001t0005g0134 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.860-2041C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144240 | |||||||
chr20:38144346 | C | T | 2 | a0001c0001t0005g0163 a0001c0001t0011g0128 |
2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.860-2147G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144346 | |||||||
chr20:38144445 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.860-2246G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144445 | |||||||
chr20:38144558 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.859+2159G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144558 | |||||||
chr20:38144618 | A | T | 1 | a0001c0004t0004g0236 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.859+2099T>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144618 | |||||||
chr20:38144643 | T | A | 5 | a0001c0006t0007g0033 a0001c0006t0007g0034 a0001c0006t0007g0279 others(2): Show |
7 | HG01167.hp1 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.859+2074A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144643 | |||||||
chr20:38144865 | G | A | 3 | a0001c0008t0008g0123 a0001c0008t0008g0129 a0001c0008t0008g0154 |
3 | HG02572.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.859+1852C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144865 | |||||||
chr20:38144890 | G | A | 70 | a0001c0001t0003g0259 a0001c0002t0001g0061 a0001c0002t0001g0067 others(67): Show |
71 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.859+1827C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144890 | |||||||
chr20:38144920 | A | G | 1 | a0001c0002t0002g0265 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.859+1797T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144920 | |||||||
chr20:38144950 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.859+1767T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144950 | |||||||
chr20:38144953 | A | G | 93 | a0001c0001t0001g0132 a0001c0001t0001g0291 a0001c0001t0002g0052 others(90): Show |
95 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.859+1764T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144953 | |||||||
chr20:38144970 | C | T | 20 | a0001c0001t0001g0132 a0001c0001t0005g0041 a0001c0001t0005g0121 others(17): Show |
21 | HG00741.hp2 HG01243.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.859+1747G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38144970 | |||||||
chr20:38145073 | G | A | 3 | a0001c0008t0008g0123 a0001c0008t0008g0129 a0001c0008t0008g0154 |
3 | HG02572.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.859+1644C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145073 | |||||||
chr20:38145184 | G | T | 1 | a0001c0003t0002g0044 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.859+1533C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145184 | |||||||
chr20:38145200 | CCAGCCTG others(4): Show |
C | 1 | a0001c0001t0001g0095 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.859+1506_859+1516d others(13): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145200 | |||||||
chr20:38145314 | G | A | 1 | a0001c0025t0004g0130 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.859+1403C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145314 | |||||||
chr20:38145431 | G | A | 1 | a0001c0001t0011g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.859+1286C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145431 | |||||||
chr20:38145473 | A | G | 3 | a0001c0002t0002g0171 a0001c0002t0002g0276 a0001c0002t0002g0286 |
3 | HG02258.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.859+1244T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145473 | |||||||
chr20:38145563 | C | T | 2 | a0002c0005t0001g0207 a0002c0005t0001g0209 |
2 | HG00621.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.859+1154G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145563 | |||||||
chr20:38145762 | C | CT | 25 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0032 others(22): Show |
27 | HG00609.hp2 HG01433.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.859+954dupA | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145762 | |||||||
chr20:38145762 | CT | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0074 others(18): Show |
23 | HG00099.hp2 HG01081.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.859+954delA | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145762 | |||||||
chr20:38145762 | CTT | C | 23 | a0001c0001t0011g0128 a0001c0002t0001g0258 a0001c0002t0002g0150 others(20): Show |
26 | HG00642.hp2 HG01261.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.859+953_859+954del others(2): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145762 | |||||||
chr20:38145762 | CTTT | C | 61 | a0001c0001t0003g0259 a0001c0001t0005g0134 a0001c0001t0005g0163 others(58): Show |
62 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.859+952_859+954del others(3): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145762 | |||||||
chr20:38145829 | G | A | 1 | a0001c0004t0004g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.859+888C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145829 | |||||||
chr20:38145841 | C | A | 27 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0059 others(24): Show |
32 | HG00609.hp2 HG02145.hp1 HG02486.hp1 others(29): Show |
intron_variant | MODIFIER | c.859+876G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145841 | |||||||
chr20:38145937 | A | G | 27 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0059 others(24): Show |
32 | HG00609.hp2 HG02145.hp1 HG02486.hp1 others(29): Show |
intron_variant | MODIFIER | c.859+780T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38145937 | |||||||
chr20:38146034 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(1): Show |
4 | HG00323.hp1 HG01934.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+683C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146034 | |||||||
chr20:38146079 | C | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0144 a0001c0001t0001g0160 others(1): Show |
6 | HG02559.hp2 HG03041.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.859+638G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146079 | |||||||
chr20:38146100 | C | T | 16 | a0001c0004t0004g0007 a0001c0004t0004g0035 a0001c0004t0004g0135 others(13): Show |
20 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.859+617G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146100 | |||||||
chr20:38146198 | C | T | 1 | a0001c0004t0004g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.859+519G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146198 | |||||||
chr20:38146353 | C | T | 2 | a0001c0001t0001g0278 a0001c0025t0004g0130 |
2 | HG02735.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.859+364G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146353 | |||||||
chr20:38146359 | A | T | 1 | a0013c0018t0001g0056 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.859+358T>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146359 | |||||||
chr20:38146409 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.859+308C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146409 | |||||||
chr20:38146447 | A | T | 1 | a0001c0001t0011g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.859+270T>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146447 | |||||||
chr20:38146448 | G | A | 97 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0059 others(94): Show |
103 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.859+269C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146448 | |||||||
chr20:38146461 | T | TG | 70 | a0001c0001t0003g0259 a0001c0002t0001g0061 a0001c0002t0001g0067 others(67): Show |
71 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.859+255dupC | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146461 | |||||||
chr20:38146496 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.859+221T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146496 | |||||||
chr20:38146595 | T | G | 1 | a0001c0002t0002g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.859+122A>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146595 | |||||||
chr20:38146622 | G | A | 29 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0059 others(26): Show |
34 | HG00609.hp2 HG02145.hp1 HG02258.hp2 others(31): Show |
intron_variant | MODIFIER | c.859+95C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146622 | |||||||
chr20:38146625 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.859+92G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146625 | |||||||
chr20:38146686 | C | T | 1 | a0001c0001t0011g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.859+31G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146686 | |||||||
chr20:38146705 | C | T | 1 | a0001c0001t0005g0134 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.859+12G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146705 | |||||||
chr20:38146711 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02735.hp1 | splice_region_variant&intron_variant | LOW | c.859+6C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 6/12 | chr20 | 38146711 | |||||||
chr20:38146941 | C | T | 1 | a0001c0001t0003g0062 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.682-47G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38146941 | |||||||
chr20:38146968 | T | C | 1 | a0001c0022t0001g0177 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.682-74A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38146968 | |||||||
chr20:38147233 | C | T | 2 | a0001c0001t0005g0134 a0001c0001t0005g0163 |
2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.682-339G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147233 | |||||||
chr20:38147316 | G | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0059 others(26): Show |
34 | HG00609.hp2 HG02145.hp1 HG02258.hp2 others(31): Show |
intron_variant | MODIFIER | c.682-422C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147316 | |||||||
chr20:38147389 | C | T | 1 | a0013c0018t0001g0056 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.682-495G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147389 | |||||||
chr20:38147409 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.682-515G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147409 | |||||||
chr20:38147533 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.681+428G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147533 | |||||||
chr20:38147561 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.681+400G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147561 | |||||||
chr20:38147599 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.681+362G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147599 | |||||||
chr20:38147702 | T | A | 29 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0059 others(26): Show |
34 | HG00609.hp2 HG02145.hp1 HG02258.hp2 others(31): Show |
intron_variant | MODIFIER | c.681+259A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147702 | |||||||
chr20:38147772 | C | T | 1 | a0001c0002t0014g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.681+189G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147772 | |||||||
chr20:38147795 | C | A | 2 | a0001c0002t0002g0124 a0001c0002t0002g0127 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.681+166G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 5/12 | chr20 | 38147795 | |||||||
chr20:38148108 | G | T | 2 | a0001c0001t0002g0162 a0001c0001t0012g0037 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.553-19C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148108 | |||||||
chr20:38148120 | G | T | 3 | a0001c0002t0002g0100 a0001c0002t0002g0103 a0001c0002t0002g0150 |
3 | HG02630.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.553-31C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148120 | |||||||
chr20:38148201 | T | G | 1 | a0001c0001t0005g0134 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.553-112A>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148201 | |||||||
chr20:38148239 | G | C | 75 | a0001c0001t0002g0052 a0001c0001t0003g0259 a0001c0001t0005g0120 others(72): Show |
78 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.553-150C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148239 | |||||||
chr20:38148538 | C | T | 1 | a0001c0002t0002g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.553-449G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148538 | |||||||
chr20:38148751 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.553-662A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148751 | |||||||
chr20:38148826 | T | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0058 others(32): Show |
44 | HG00140.hp2 HG00609.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.553-737A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148826 | |||||||
chr20:38148885 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.553-796G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148885 | |||||||
chr20:38148885 | C | T | 1 | a0001c0001t0011g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.553-796G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148885 | |||||||
chr20:38148886 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.553-797T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148886 | |||||||
chr20:38148890 | G | C | 1 | a0001c0001t0001g0095 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.553-801C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148890 | |||||||
chr20:38148991 | G | C | 1 | a0001c0002t0002g0172 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.553-902C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38148991 | |||||||
chr20:38149007 | G | A | 3 | a0001c0008t0008g0123 a0001c0008t0008g0129 a0001c0008t0008g0154 |
3 | HG02572.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.553-918C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149007 | |||||||
chr20:38149020 | G | A | 29 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0059 others(26): Show |
34 | HG00609.hp2 HG02145.hp1 HG02258.hp2 others(31): Show |
intron_variant | MODIFIER | c.553-931C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149020 | |||||||
chr20:38149060 | T | C | 73 | a0001c0001t0003g0259 a0001c0002t0001g0061 a0001c0002t0001g0067 others(70): Show |
76 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.553-971A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149060 | |||||||
chr20:38149104 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0009g0299 |
2 | HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.553-1015G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149104 | |||||||
chr20:38149213 | A | G | 1 | a0001c0002t0002g0246 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.553-1124T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149213 | |||||||
chr20:38149415 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.553-1326G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149415 | |||||||
chr20:38149505 | G | A | 20 | a0001c0001t0001g0132 a0001c0001t0005g0041 a0001c0001t0005g0120 others(17): Show |
21 | HG00741.hp2 HG01243.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.553-1416C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149505 | |||||||
chr20:38149525 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.552+1414T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149525 | |||||||
chr20:38149551 | C | T | 2 | a0001c0001t0002g0162 a0001c0001t0012g0037 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.552+1388G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149551 | |||||||
chr20:38149627 | C | T | 2 | a0001c0002t0006g0137 a0001c0002t0006g0141 |
2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.552+1312G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149627 | |||||||
chr20:38149678 | C | CA | 17 | a0001c0001t0001g0017 a0001c0001t0001g0057 a0001c0001t0001g0096 others(14): Show |
19 | HG00099.hp2 HG00733.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.552+1260dupT | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0002g0248 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.552+1251_552+1260d others(12): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0002g0267 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.552+1250_552+1260d others(13): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(5): Show |
3 | a0001c0002t0002g0100 a0001c0002t0002g0238 a0001c0002t0002g0249 |
3 | HG01496.hp1 HG02004.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.552+1249_552+1260d others(14): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(6): Show |
3 | a0001c0002t0002g0042 a0001c0002t0002g0272 a0001c0002t0002g0292 |
3 | HG01981.hp1 HG02300.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.552+1248_552+1260d others(15): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(7): Show |
1 | a0001c0004t0004g0168 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.552+1247_552+1260d others(16): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(8): Show |
2 | a0001c0004t0004g0135 a0001c0004t0004g0169 |
2 | HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.552+1246_552+1260d others(17): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(9): Show |
5 | a0001c0004t0004g0007 a0001c0004t0004g0187 a0001c0004t0004g0192 others(2): Show |
7 | HG01167.hp1 HG01261.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+1245_552+1260d others(18): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(10): Show |
7 | a0001c0001t0002g0162 a0001c0001t0011g0128 a0001c0004t0004g0140 others(4): Show |
8 | HG02055.hp1 HG02145.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+1244_552+1260d others(19): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(11): Show |
1 | a0001c0004t0010g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.552+1243_552+1260d others(20): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0012g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.552+1241_552+1260d others(22): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(18): Show |
10 | a0001c0002t0001g0061 a0001c0002t0001g0067 a0001c0002t0002g0039 others(7): Show |
10 | HG00609.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.552+1260_552+1261i others(27): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(19): Show |
18 | a0001c0002t0002g0031 a0001c0002t0002g0040 a0001c0002t0002g0068 others(15): Show |
19 | HG00642.hp2 HG01071.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.552+1260_552+1261i others(28): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(20): Show |
11 | a0001c0001t0003g0259 a0001c0002t0001g0258 a0001c0002t0002g0043 others(8): Show |
11 | HG00423.hp2 HG03098.hp1 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.552+1260_552+1261i others(29): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(21): Show |
1 | a0001c0002t0002g0260 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.552+1260_552+1261i others(30): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(22): Show |
7 | a0001c0001t0001g0125 a0001c0002t0002g0242 a0001c0002t0002g0261 others(4): Show |
7 | HG00597.hp2 HG00733.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+1260_552+1261i others(31): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(23): Show |
2 | a0001c0007t0002g0270 a0006c0020t0002g0069 |
2 | HG01123.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.552+1260_552+1261i others(32): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(24): Show |
2 | a0001c0002t0002g0102 a0001c0026t0002g0186 |
2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.552+1260_552+1261i others(33): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0005g0134 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.552+1260_552+1261i others(34): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(26): Show |
2 | a0001c0002t0002g0265 a0007c0019t0002g0050 |
2 | HG02886.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.552+1260_552+1261i others(35): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(28): Show |
2 | a0001c0002t0002g0103 a0001c0002t0002g0150 |
2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.552+1260_552+1261i others(37): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | C | CAAAAAAA others(29): Show |
1 | a0001c0002t0002g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.552+1260_552+1261i others(38): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149678 | CA | C | 18 | a0001c0001t0001g0020 a0001c0001t0001g0054 a0001c0001t0001g0059 others(15): Show |
22 | HG01243.hp2 HG01515.hp2 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.552+1260delT | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149678 | |||||||
chr20:38149690 | A | AAAAAAAA others(11): Show |
1 | a0001c0002t0011g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.552+1248_552+1249i others(20): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149690 | |||||||
chr20:38149690 | A | AAAAAAAA others(9): Show |
1 | a0001c0009t0007g0277 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.552+1248_552+1249i others(18): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149690 | |||||||
chr20:38149690 | A | AAAAAAAA others(6): Show |
2 | a0001c0006t0007g0033 a0001c0006t0007g0034 |
4 | HG02809.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+1248_552+1249i others(15): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149690 | |||||||
chr20:38149690 | A | AAAAAAAA others(5): Show |
1 | a0001c0006t0007g0279 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.552+1237_552+1248d others(14): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149690 | |||||||
chr20:38149692 | A | AAAAAAAA others(11): Show |
1 | a0001c0003t0002g0202 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.552+1246_552+1247i others(20): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149692 | |||||||
chr20:38149692 | A | AAAAAAAA others(10): Show |
2 | a0001c0001t0001g0058 a0012c0015t0002g0185 |
2 | HG04228.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.552+1246_552+1247i others(19): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149692 | |||||||
chr20:38149692 | A | AAAAAAAA others(9): Show |
8 | a0001c0001t0004g0193 a0001c0002t0002g0286 a0001c0003t0002g0026 others(5): Show |
9 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+1246_552+1247i others(18): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149692 | |||||||
chr20:38149692 | A | AAAAAAAA others(8): Show |
13 | a0001c0001t0001g0133 a0001c0001t0001g0200 a0001c0002t0002g0276 others(10): Show |
16 | HG03710.hp1 HG06807.hp2 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.552+1246_552+1247i others(17): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149692 | |||||||
chr20:38149692 | A | AAAAAAAA others(7): Show |
1 | a0003c0012t0002g0227 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.552+1246_552+1247i others(16): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149692 | |||||||
chr20:38149692 | A | C | 2 | a0001c0008t0008g0129 a0001c0008t0008g0154 |
2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.552+1247T>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149692 | |||||||
chr20:38149713 | G | A | 67 | a0001c0001t0001g0125 a0001c0001t0003g0259 a0001c0002t0001g0061 others(64): Show |
68 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.552+1226C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149713 | |||||||
chr20:38149719 | A | G | 1 | a0001c0001t0011g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.552+1220T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149719 | |||||||
chr20:38149824 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0048 |
4 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+1115G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38149824 | |||||||
chr20:38150208 | T | C | 55 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(52): Show |
62 | HG00597.hp1 HG00609.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.552+731A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38150208 | |||||||
chr20:38150222 | C | T | 2 | a0001c0004t0004g0168 a0001c0004t0004g0169 |
2 | HG01109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.552+717G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38150222 | |||||||
chr20:38150547 | C | G | 2 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.552+392G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38150547 | |||||||
chr20:38150741 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.552+198C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38150741 | |||||||
chr20:38150882 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0005g0134 |
2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.552+57C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 4/12 | chr20 | 38150882 | |||||||
chr20:38151182 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.434-125T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38151182 | |||||||
chr20:38151368 | C | G | 6 | a0001c0001t0001g0125 a0001c0001t0001g0164 a0001c0002t0002g0171 others(3): Show |
6 | HG01109.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.434-311G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38151368 | |||||||
chr20:38151378 | G | C | 1 | a0001c0002t0017g0205 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.434-321C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38151378 | |||||||
chr20:38151426 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0005g0134 a0001c0002t0011g0126 |
3 | HG01884.hp2 HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.434-369T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38151426 | |||||||
chr20:38151449 | C | T | 1 | a0001c0001t0009g0296 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.434-392G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38151449 | |||||||
chr20:38151605 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.434-548C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38151605 | |||||||
chr20:38151711 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(97): Show |
123 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.434-654C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38151711 | |||||||
chr20:38151901 | G | A | 21 | a0001c0001t0001g0058 a0001c0001t0001g0133 a0001c0001t0001g0200 others(18): Show |
23 | HG01361.hp2 HG02145.hp1 HG03579.hp2 others(20): Show |
intron_variant | MODIFIER | c.434-844C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38151901 | |||||||
chr20:38151949 | C | T | 1 | a0001c0002t0002g0240 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.434-892G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38151949 | |||||||
chr20:38152142 | T | G | 1 | a0001c0001t0009g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.434-1085A>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152142 | |||||||
chr20:38152247 | G | A | 3 | a0001c0001t0005g0120 a0001c0006t0007g0034 a0001c0006t0007g0279 |
4 | HG02723.hp2 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-1190C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152247 | |||||||
chr20:38152321 | T | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0144 a0001c0001t0001g0148 others(2): Show |
7 | HG02055.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-1264A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152321 | |||||||
chr20:38152350 | A | T | 84 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0281 others(81): Show |
91 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.434-1293T>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152350 | |||||||
chr20:38152449 | G | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(97): Show |
123 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.434-1392C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152449 | |||||||
chr20:38152460 | A | G | 91 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0125 others(88): Show |
98 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.434-1403T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152460 | |||||||
chr20:38152488 | T | C | 4 | a0001c0001t0001g0125 a0001c0004t0004g0135 a0001c0004t0004g0168 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-1431A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152488 | |||||||
chr20:38152647 | T | C | 3 | a0001c0001t0001g0059 a0001c0001t0019g0298 a0001c0002t0014g0060 |
3 | HG02451.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.434-1590A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152647 | |||||||
chr20:38152783 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.434-1726T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152783 | |||||||
chr20:38152795 | G | A | 2 | a0001c0001t0001g0114 a0001c0007t0002g0271 |
2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.434-1738C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152795 | |||||||
chr20:38152938 | C | T | 8 | a0001c0002t0002g0031 a0001c0002t0002g0173 a0001c0002t0002g0237 others(5): Show |
9 | NA18944.hp1 NA18981.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.434-1881G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152938 | |||||||
chr20:38152991 | T | C | 1 | a0001c0002t0002g0266 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.434-1934A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38152991 | |||||||
chr20:38153038 | CG | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0020 others(127): Show |
150 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.434-1982delC | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153038 | |||||||
chr20:38153042 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.434-1985C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153042 | |||||||
chr20:38153162 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.434-2105G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153162 | |||||||
chr20:38153217 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.434-2160G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153217 | |||||||
chr20:38153247 | G | C | 38 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0030 others(35): Show |
45 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.434-2190C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153247 | |||||||
chr20:38153297 | G | A | 93 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0125 others(90): Show |
100 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.434-2240C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153297 | |||||||
chr20:38153334 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02080.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.434-2277C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153334 | |||||||
chr20:38153449 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0019g0298 a0001c0002t0014g0060 |
3 | HG02451.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.434-2392G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153449 | |||||||
chr20:38153476 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0113 |
2 | HG01099.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.433+2371C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153476 | |||||||
chr20:38153528 | A | AAAAAAAA others(14): Show |
5 | a0001c0001t0005g0134 a0001c0002t0002g0267 a0001c0002t0011g0126 others(2): Show |
5 | HG01891.hp2 NA18943.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.433+2318_433+2319i others(23): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153528 | A | AAAAAAAA others(13): Show |
77 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0125 others(74): Show |
83 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.433+2318_433+2319i others(22): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153528 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0012g0037 a0001c0002t0002g0238 |
2 | HG01496.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.433+2318_433+2319i others(21): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153528 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.433+2318_433+2319i others(24): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153528 | A | AAAAAAAA others(14): Show |
17 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0138 others(14): Show |
24 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.433+2318_433+2319i others(23): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153528 | A | AAAAAAAA others(13): Show |
1 | a0001c0004t0004g0035 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.433+2318_433+2319i others(22): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153528 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0005g0163 a0004c0013t0005g0024 |
3 | HG01243.hp2 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.433+2318_433+2319i others(21): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153528 | A | AAAAAGAA others(14): Show |
3 | a0001c0001t0001g0059 a0001c0001t0019g0298 a0001c0002t0014g0060 |
3 | HG02451.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.433+2318_433+2319i others(23): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153528 | A | AAAAAGAA others(13): Show |
73 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0028 others(70): Show |
88 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.433+2318_433+2319i others(22): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153528 | A | G | 1 | a0001c0001t0005g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433+2319T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153528 | |||||||
chr20:38153533 | G | A | 1 | a0001c0002t0002g0237 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.433+2314C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153533 | |||||||
chr20:38153534 | A | AAAAAAAA others(12): Show |
3 | a0001c0001t0001g0217 a0001c0002t0002g0127 a0001c0002t0002g0237 |
3 | HG01517.hp1 HG02717.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.433+2312_433+2313i others(21): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153534 | |||||||
chr20:38153547 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.433+2300C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153547 | |||||||
chr20:38153562 | T | C | 1 | a0001c0003t0002g0044 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.433+2285A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153562 | |||||||
chr20:38153616 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.433+2231G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153616 | |||||||
chr20:38153631 | T | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0228 a0001c0001t0001g0229 |
4 | HG01175.hp1 HG01433.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+2216A>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153631 | |||||||
chr20:38153643 | G | T | 78 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0028 others(75): Show |
93 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.433+2204C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153643 | |||||||
chr20:38153728 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0019g0298 a0001c0002t0014g0060 |
3 | HG02451.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.433+2119C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153728 | |||||||
chr20:38153814 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0005g0134 a0001c0002t0011g0126 |
3 | HG01884.hp2 HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.433+2033G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38153814 | |||||||
chr20:38154171 | C | T | 6 | a0001c0001t0001g0125 a0001c0001t0001g0164 a0001c0002t0002g0171 others(3): Show |
6 | HG01109.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.433+1676G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38154171 | |||||||
chr20:38154327 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.433+1520A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38154327 | |||||||
chr20:38154502 | C | G | 5 | a0001c0001t0005g0041 a0001c0002t0006g0010 a0001c0002t0006g0023 others(2): Show |
8 | HG00741.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.433+1345G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38154502 | |||||||
chr20:38154643 | G | T | 2 | a0001c0003t0002g0194 a0001c0003t0002g0195 |
2 | NA18980.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.433+1204C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38154643 | |||||||
chr20:38154645 | A | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(196): Show |
230 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.433+1202T>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38154645 | |||||||
chr20:38154712 | G | A | 1 | a0001c0002t0002g0014 | 3 | HG00280.hp2 HG00323.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.433+1135C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38154712 | |||||||
chr20:38154716 | T | C | 1 | a0001c0002t0002g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.433+1131A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38154716 | |||||||
chr20:38154754 | C | A | 2 | a0001c0003t0002g0045 a0001c0003t0002g0046 |
2 | NA18945.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.433+1093G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38154754 | |||||||
chr20:38154949 | T | C | 1 | a0003c0012t0020g0300 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.433+898A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38154949 | |||||||
chr20:38155065 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0005g0134 a0001c0002t0011g0126 |
3 | HG01884.hp2 HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.433+782G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155065 | |||||||
chr20:38155081 | A | G | 89 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0028 others(86): Show |
106 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.433+766T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155081 | |||||||
chr20:38155107 | A | AAAAAC | 85 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0281 others(82): Show |
92 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.433+735_433+739dup others(5): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155107 | |||||||
chr20:38155132 | A | G | 1 | a0001c0004t0004g0236 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.433+715T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155132 | |||||||
chr20:38155180 | T | C | 171 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0028 others(168): Show |
194 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(191): Show |
intron_variant | MODIFIER | c.433+667A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155180 | |||||||
chr20:38155197 | T | G | 75 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(72): Show |
88 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.433+650A>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155197 | |||||||
chr20:38155440 | C | A | 1 | a0001c0002t0002g0272 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.433+407G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155440 | |||||||
chr20:38155554 | A | G | 2 | a0001c0001t0004g0193 a0003c0012t0020g0300 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.433+293T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155554 | |||||||
chr20:38155603 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433+244G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155603 | |||||||
chr20:38155644 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.433+203C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 3/12 | chr20 | 38155644 | |||||||
chr20:38156284 | A | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0059 others(38): Show |
49 | HG00738.hp2 HG00741.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.191-195T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38156284 | |||||||
chr20:38156368 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0020 others(143): Show |
169 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.191-279A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38156368 | |||||||
chr20:38156654 | T | A | 1 | a0001c0027t0001g0170 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.191-565A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38156654 | |||||||
chr20:38156725 | G | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0138 others(14): Show |
25 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.191-636C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38156725 | |||||||
chr20:38156822 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.191-733C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38156822 | |||||||
chr20:38157004 | C | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0153 a0001c0001t0001g0155 others(4): Show |
9 | HG00738.hp2 HG01167.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.191-915G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157004 | |||||||
chr20:38157226 | C | A | 3 | a0001c0001t0011g0128 a0001c0008t0008g0129 a0001c0025t0004g0130 |
3 | HG02145.hp2 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.191-1137G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157226 | |||||||
chr20:38157274 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.191-1185G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157274 | |||||||
chr20:38157284 | C | T | 1 | a0001c0001t0005g0134 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.191-1195G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157284 | |||||||
chr20:38157373 | T | G | 3 | a0001c0001t0011g0128 a0001c0008t0008g0129 a0001c0025t0004g0130 |
3 | HG02145.hp2 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.191-1284A>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157373 | |||||||
chr20:38157416 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.191-1327G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157416 | |||||||
chr20:38157470 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.191-1381T>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157470 | |||||||
chr20:38157532 | A | G | 127 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0051 others(124): Show |
142 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.191-1443T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157532 | |||||||
chr20:38157560 | T | C | 1 | a0001c0011t0001g0019 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.191-1471A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157560 | |||||||
chr20:38157627 | A | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0020 others(145): Show |
171 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.191-1538T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157627 | |||||||
chr20:38157724 | A | C | 127 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0051 others(124): Show |
142 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.191-1635T>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157724 | |||||||
chr20:38157755 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0119 |
3 | HG00558.hp1 HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.191-1666G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157755 | |||||||
chr20:38157827 | T | C | 3 | a0001c0001t0011g0128 a0001c0008t0008g0129 a0001c0025t0004g0130 |
3 | HG02145.hp2 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.191-1738A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157827 | |||||||
chr20:38157939 | G | A | 1 | a0001c0003t0002g0231 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.191-1850C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157939 | |||||||
chr20:38157983 | G | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0232 |
2 | HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.191-1894C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38157983 | |||||||
chr20:38158077 | T | C | 4 | a0001c0001t0005g0161 a0001c0001t0005g0163 a0001c0027t0001g0170 others(1): Show |
5 | HG01243.hp2 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-1988A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38158077 | |||||||
chr20:38158168 | G | A | 5 | a0001c0001t0001g0125 a0001c0002t0002g0171 a0001c0002t0011g0126 others(2): Show |
5 | HG01109.hp1 HG02965.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-2079C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38158168 | |||||||
chr20:38158202 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.191-2113G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38158202 | |||||||
chr20:38158323 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.191-2234C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38158323 | |||||||
chr20:38158585 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
154 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.191-2496T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38158585 | |||||||
chr20:38159027 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.190+2393C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159027 | |||||||
chr20:38159064 | G | T | 1 | a0001c0002t0002g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.190+2356C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159064 | |||||||
chr20:38159093 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.190+2327C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159093 | |||||||
chr20:38159157 | C | T | 1 | a0001c0002t0002g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.190+2263G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159157 | |||||||
chr20:38159400 | G | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.190+2020C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159400 | |||||||
chr20:38159520 | A | T | 1 | a0001c0027t0001g0170 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.190+1900T>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159520 | |||||||
chr20:38159522 | AAAAG | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.190+1894_190+1897d others(6): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159522 | |||||||
chr20:38159712 | C | A | 1 | a0001c0001t0001g0233 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.190+1708G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159712 | |||||||
chr20:38159789 | A | G | 76 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(73): Show |
89 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.190+1631T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159789 | |||||||
chr20:38159973 | A | G | 1 | a0003c0012t0020g0300 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.190+1447T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38159973 | |||||||
chr20:38160382 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.190+1038A>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38160382 | |||||||
chr20:38161006 | C | T | 1 | a0001c0026t0002g0186 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.190+414G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38161006 | |||||||
chr20:38161023 | T | C | 2 | a0001c0002t0002g0171 a0001c0027t0001g0170 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.190+397A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38161023 | |||||||
chr20:38161113 | G | A | 1 | a0001c0002t0002g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.190+307C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38161113 | |||||||
chr20:38161208 | A | G | 2 | a0001c0002t0002g0039 a0001c0002t0002g0040 |
2 | NA18952.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.190+212T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38161208 | |||||||
chr20:38161368 | G | C | 1 | a0001c0002t0002g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.190+52C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 2/12 | chr20 | 38161368 | |||||||
chr20:38161726 | G | A | 1 | a0001c0001t0009g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.11-127C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38161726 | |||||||
chr20:38161764 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.11-165T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38161764 | |||||||
chr20:38161891 | T | C | 1 | a0001c0002t0002g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.11-292A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38161891 | |||||||
chr20:38162145 | C | T | 2 | a0001c0003t0002g0182 a0001c0003t0002g0183 |
2 | NA18974.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.11-546G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38162145 | |||||||
chr20:38162723 | C | A | 1 | a0001c0001t0001g0287 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.11-1124G>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38162723 | |||||||
chr20:38162770 | G | A | 1 | a0001c0001t0013g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.11-1171C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38162770 | |||||||
chr20:38162792 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.11-1193C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38162792 | |||||||
chr20:38162802 | G | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.11-1203C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38162802 | |||||||
chr20:38162891 | A | G | 4 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0002t0002g0178 others(1): Show |
4 | NA18952.hp2 NA18957.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.11-1292T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38162891 | |||||||
chr20:38162911 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.11-1312A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38162911 | |||||||
chr20:38162912 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.11-1313C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38162912 | |||||||
chr20:38162954 | C | G | 8 | a0001c0001t0001g0125 a0001c0001t0005g0120 a0001c0001t0005g0121 others(5): Show |
8 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.11-1355G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38162954 | |||||||
chr20:38163094 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.11-1495G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163094 | |||||||
chr20:38163095 | G | A | 1 | a0001c0002t0002g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.11-1496C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163095 | |||||||
chr20:38163141 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.11-1542G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163141 | |||||||
chr20:38163194 | C | T | 1 | a0001c0022t0001g0177 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.11-1595G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163194 | |||||||
chr20:38163217 | G | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.11-1618C>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163217 | |||||||
chr20:38163254 | A | ACT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.11-1657_11-1656dup others(2): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163254 | |||||||
chr20:38163426 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.10+1763C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163426 | |||||||
chr20:38163447 | C | G | 2 | a0001c0002t0002g0294 a0001c0004t0004g0293 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.10+1742G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163447 | |||||||
chr20:38163456 | T | C | 1 | a0001c0001t0012g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.10+1733A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163456 | |||||||
chr20:38163601 | T | C | 2 | a0001c0001t0001g0291 a0001c0004t0004g0035 |
3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.10+1588A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163601 | |||||||
chr20:38163632 | C | T | 2 | a0001c0001t0003g0174 a0001c0001t0003g0175 |
2 | NA18942.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.10+1557G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163632 | |||||||
chr20:38163646 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.10+1543C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163646 | |||||||
chr20:38163721 | A | T | 1 | a0001c0001t0013g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.10+1468T>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163721 | |||||||
chr20:38163772 | C | T | 1 | a0001c0002t0002g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.10+1417G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38163772 | |||||||
chr20:38164043 | T | C | 1 | a0001c0002t0002g0292 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.10+1146A>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38164043 | |||||||
chr20:38164155 | C | T | 7 | a0001c0001t0001g0125 a0001c0001t0005g0120 a0001c0001t0005g0121 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.10+1034G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38164155 | |||||||
chr20:38164440 | A | G | 13 | a0001c0001t0009g0295 a0001c0001t0009g0296 a0001c0001t0009g0299 others(10): Show |
14 | HG01261.hp1 HG02145.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.10+749T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38164440 | |||||||
chr20:38164440 | A | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(87): Show |
108 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.10+749T>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38164440 | |||||||
chr20:38164500 | C | T | 1 | a0001c0002t0002g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.10+689G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38164500 | |||||||
chr20:38164651 | C | T | 1 | a0001c0002t0002g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.10+538G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38164651 | |||||||
chr20:38164773 | TTGCACAC others(13): Show |
T | 1 | a0001c0002t0002g0173 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.10+396_10+415delTG others(18): Show |
TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38164773 | |||||||
chr20:38164843 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.10+346G>A | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38164843 | |||||||
chr20:38165047 | A | C | 7 | a0001c0001t0001g0125 a0001c0001t0005g0120 a0001c0001t0005g0121 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.10+142T>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38165047 | |||||||
chr20:38165099 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.10+90T>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38165099 | |||||||
chr20:38165119 | C | G | 1 | a0001c0001t0009g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.10+70G>C | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38165119 | |||||||
chr20:38165127 | G | A | 136 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(133): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.10+62C>T | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38165127 | |||||||
chr20:38165149 | G | C | 2 | a0001c0002t0002g0294 a0001c0004t0004g0293 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.10+40C>G | TGM2 | ENSG00000198959.12 | transcript | ENST00000361475.7 | protein_coding | 1/12 | chr20 | 38165149 |