Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51095 |
| ensemblid | ENSG00000072756.18 |
| hgncid | 17341 |
| symbol | TRNT1 |
| name | tRNA nucleotidyl transferase 1 |
| refseq_nuc | NM_182916.3 |
| refseq_prot | NP_886552.3 |
| ensembl_nuc | ENST00000251607.11 |
| ensembl_prot | ENSP00000251607.6 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 3126940 |
| end | 3149023 |
| strand | + |
| ver | v1.2 |
| region | chr3:3126940-3149023 |
| region5000 | chr3:3121940-3154023 |
| regionname0 | TRNT1_chr3_3126940_3149023 |
| regionname5000 | TRNT1_chr3_3121940_3154023 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 434 | 366 | 62 | 73 | 175 | 12 | 43 | 135 | TRNT1_chr3_3121940_3154023 | TRNT1 | MLRCL others(429): Show |
chr3 | 3121940 | 3154023 |
| a0002 | 1/0 | 434 | 31 | 28 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | MLRCL others(429): Show |
chr3 | 3121940 | 3154023 |
| a0003 | 0/0 | 434 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | MLRCL others(429): Show |
chr3 | 3121940 | 3154023 |
| a0004 | 0/0 | 434 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | MLRCL others(429): Show |
chr3 | 3121940 | 3154023 |
| a0005 | 0/0 | 434 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | MLRCL others(429): Show |
chr3 | 3121940 | 3154023 |
| a0006 | 0/0 | 367 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | MLRCL others(362): Show |
chr3 | 3121940 | 3154023 |
| a0007 | 0/0 | 434 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | MLRCL others(429): Show |
chr3 | 3121940 | 3154023 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1302 | 304 | 45 | 52 | 163 | 9 | 34 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0001c0002 | 0/0 | 1302 | 54 | 10 | 21 | 11 | 3 | 9 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0001c0004 | 0/0 | 1302 | 6 | 6 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0001c0010 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0001c0012 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0002c0003 | 1/0 | 1302 | 25 | 23 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0002c0005 | 0/0 | 1302 | 4 | 3 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0002c0006 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0002c0008 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0003c0014 | 0/0 | 1302 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0004c0013 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0005c0007 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0006c0011 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 | ||
| a0007c0009 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | ATGCT others(1297): Show |
chr3 | 3121940 | 3154023 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2271 | 163 | 10 | 18 | 115 | 2 | 18 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0002 | 0/1 | 2271 | 80 | 14 | 24 | 27 | 6 | 8 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0003 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0005 | 0/0 | 2272 | 18 | 3 | 7 | 2 | 0 | 6 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2267): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0006 | 0/0 | 2267 | 12 | 3 | 0 | 8 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2262): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0007 | 0/0 | 2275 | 7 | 4 | 1 | 0 | 0 | 2 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2270): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0009 | 0/0 | 2275 | 5 | 5 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2270): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0011 | 0/0 | 2271 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0012 | 0/0 | 2271 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0013 | 0/0 | 2271 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0017 | 0/0 | 2267 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2262): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0018 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0021 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0022 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0024 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0001t0025 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0002t0003 | 0/0 | 2252 | 50 | 7 | 21 | 10 | 3 | 9 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0001c0002t0014 | 0/0 | 2252 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0001c0002t0019 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2251): Show |
chr3 | 3121940 | 3154023 |
| a0001c0002t0020 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0001c0004t0008 | 0/0 | 2252 | 5 | 5 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGACC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0001c0004t0016 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGACC others(2251): Show |
chr3 | 3121940 | 3154023 |
| a0001c0010t0001 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0001c0012t0003 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0002c0003t0004 | 1/0 | 2252 | 21 | 19 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0002c0003t0015 | 0/0 | 2252 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0002c0003t0023 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0002c0005t0010 | 0/0 | 2272 | 4 | 3 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2267): Show |
chr3 | 3121940 | 3154023 |
| a0002c0006t0010 | 0/0 | 2272 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2267): Show |
chr3 | 3121940 | 3154023 |
| a0002c0008t0004 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0003c0014t0016 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGACC others(2251): Show |
chr3 | 3121940 | 3154023 |
| a0004c0013t0026 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2262): Show |
chr3 | 3121940 | 3154023 |
| a0005c0007t0014 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2247): Show |
chr3 | 3121940 | 3154023 |
| a0006c0011t0001 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| a0007c0009t0002 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | AGCCC others(2266): Show |
chr3 | 3121940 | 3154023 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 56 | 3 | 9 | 38 | 1 | 5 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0004 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0006 | 0/0 | 12 | 1 | 1 | 9 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0008 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0009 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0005 | 0/0 | 13 | 2 | 4 | 5 | 2 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0007 | 0/0 | 12 | 1 | 9 | 0 | 2 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0012 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0010 | 0/0 | 8 | 1 | 5 | 1 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0006g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0006g0024 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0007g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0009g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0011g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0012g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0017g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0017g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0018g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0021g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0022g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0024g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0001t0025g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0002 | 0/0 | 23 | 3 | 4 | 7 | 3 | 6 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0011 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0014 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0014g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0019g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0002t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0004t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0004t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0004t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0004t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0004t0016g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0010t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0001c0012t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0003t0004g0003 | 1/0 | 12 | 10 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0003t0004g0017 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0003t0004g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0003t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0003t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0003t0015g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0003t0023g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0005t0010g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0005t0010g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0006t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0002c0008t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0003c0014t0016g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0004c0013t0026g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0005c0007t0014g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0006c0011t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| a0007c0009t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0002 | EUR | GBR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0024 | EUR | FIN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0002 | EUR | FIN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0134 | EUR | FIN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00642 | hp2 | a0003 | c0014 | t0016 | g0151 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0041 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0136 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01106 | hp2 | a0001 | c0001 | t0017 | g0052 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01167 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0042 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0096 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01175 | hp2 | a0001 | c0001 | t0017 | g0051 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01243 | hp1 | a0002 | c0003 | t0004 | g0003 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01243 | hp2 | a0002 | c0005 | t0010 | g0159 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0145 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0150 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0002 | EUR | IBS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01884 | hp2 | a0001 | c0004 | t0008 | g0023 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01891 | hp1 | a0001 | c0004 | t0008 | g0023 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01891 | hp2 | a0001 | c0001 | t0013 | g0095 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0146 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01978 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0141 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02055 | hp2 | a0002 | c0003 | t0004 | g0043 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02135 | hp2 | a0001 | c0001 | t0021 | g0006 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02155 | hp2 | a0001 | c0002 | t0020 | g0002 | EAS | CDX | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0129 | EAS | CDX | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02257 | hp1 | a0002 | c0003 | t0004 | g0003 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02257 | hp2 | a0001 | c0004 | t0008 | g0046 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02258 | hp1 | a0004 | c0013 | t0026 | g0098 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02258 | hp2 | a0002 | c0008 | t0004 | g0003 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02280 | hp2 | a0001 | c0012 | t0003 | g0153 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0142 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02615 | hp1 | a0002 | c0003 | t0004 | g0003 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02622 | hp1 | a0001 | c0004 | t0016 | g0152 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02622 | hp2 | a0002 | c0003 | t0004 | g0157 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02647 | hp1 | a0002 | c0003 | t0004 | g0017 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0130 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0137 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0068 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02723 | hp1 | a0002 | c0003 | t0004 | g0017 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0033 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0097 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02886 | hp1 | a0002 | c0003 | t0004 | g0003 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02895 | hp1 | a0001 | c0002 | t0003 | g0149 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02895 | hp2 | a0002 | c0003 | t0004 | g0003 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02896 | hp1 | a0001 | c0001 | t0013 | g0022 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02896 | hp2 | a0002 | c0003 | t0004 | g0017 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0033 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02922 | hp1 | a0002 | c0003 | t0004 | g0017 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02965 | hp2 | a0002 | c0003 | t0015 | g0003 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02970 | hp1 | a0002 | c0003 | t0004 | g0043 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02976 | hp1 | a0002 | c0003 | t0004 | g0003 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02976 | hp2 | a0002 | c0003 | t0015 | g0003 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03041 | hp2 | a0005 | c0007 | t0014 | g0138 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03098 | hp1 | a0001 | c0001 | t0018 | g0049 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03130 | hp1 | a0002 | c0005 | t0010 | g0019 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03130 | hp2 | a0001 | c0004 | t0008 | g0045 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03195 | hp2 | a0001 | c0001 | t0025 | g0121 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03209 | hp1 | a0001 | c0002 | t0014 | g0039 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0042 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03453 | hp1 | a0002 | c0003 | t0023 | g0003 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03453 | hp2 | a0002 | c0005 | t0010 | g0019 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03486 | hp2 | a0002 | c0003 | t0004 | g0158 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0055 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0056 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03516 | hp2 | a0002 | c0003 | t0015 | g0003 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0140 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03579 | hp2 | a0001 | c0004 | t0008 | g0044 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0143 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03927 | hp1 | a0006 | c0011 | t0001 | g0085 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0054 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0144 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18522 | hp2 | a0002 | c0006 | t0010 | g0019 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18612 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | CHB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18906 | hp1 | a0002 | c0003 | t0004 | g0003 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0034 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18944 | hp1 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18952 | hp2 | a0001 | c0010 | t0001 | g0083 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18961 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18967 | hp2 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18969 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18978 | hp2 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18990 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18995 | hp1 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19030 | hp2 | a0002 | c0003 | t0004 | g0003 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19060 | hp1 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19060 | hp2 | a0001 | c0001 | t0022 | g0091 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19066 | hp2 | a0007 | c0009 | t0002 | g0005 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19076 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19077 | hp2 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19084 | hp1 | a0001 | c0001 | t0012 | g0108 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19085 | hp2 | a0001 | c0001 | t0024 | g0009 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA19240 | hp2 | a0002 | c0005 | t0010 | g0019 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ASW | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ASW | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | TSI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02109 | hp2 | a0001 | c0002 | t0014 | g0039 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG02559 | hp2 | a0002 | c0003 | t0004 | g0003 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03471 | hp1 | a0002 | c0003 | t0004 | g0017 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG03471 | hp2 | a0002 | c0003 | t0004 | g0003 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | USA | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | USA | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA20300 | hp1 | a0002 | c0003 | t0004 | g0003 | AFR | USA | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | USA | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA21309 | hp1 | a0001 | c0002 | t0019 | g0002 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0160 | REF | REF | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0004 | g0003 | REF | REF | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3129108 | C | T | 5 | a0001 a0003 a0004 others(2): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
missense_variant | MODERATE | c.68C>T | p.Pro23Leu | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/8 | 146/2252 | 68/1305 | 23/434 | chr3 | 3129108 | |||
| chr3:3137442 | A | G | 1 | a0004 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.331A>G | p.Ile111Val | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/8 | 409/2252 | 331/1305 | 111/434 | chr3 | 3137442 | |||
| chr3:3137452 | G | A | 1 | a0007 | 1 | NA19066.hp2 | missense_variant&splice_region_variant | MODERATE | c.341G>A | p.Arg114Lys | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/8 | 419/2252 | 341/1305 | 114/434 | chr3 | 3137452 | |||
| chr3:3147495 | A | G | 1 | a0003 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.848A>G | p.Lys283Arg | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/8 | 926/2252 | 848/1305 | 283/434 | chr3 | 3147495 | |||
| chr3:3147509 | T | A | 1 | a0005 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.862T>A | p.Phe288Ile | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/8 | 940/2252 | 862/1305 | 288/434 | chr3 | 3147509 | |||
| chr3:3147953 | C | G | 1 | a0006 | 1 | HG03927.hp1 | stop_gained | HIGH | c.1104C>G | p.Tyr368* | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 1182/2252 | 1104/1305 | 368/434 | chr3 | 3147953 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3129173 | C | T | 2 | a0001c0004 a0003c0014 |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
synonymous_variant | LOW | c.133C>T | p.Leu45Leu | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/8 | 211/2252 | 133/1305 | 45/434 | chr3 | 3129173 | |||
| chr3:3140611 | G | T | 3 | a0001c0004 a0001c0012 a0003c0014 |
8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
synonymous_variant | LOW | c.444G>T | p.Ala148Ala | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/8 | 522/2252 | 444/1305 | 148/434 | chr3 | 3140611 | |||
| chr3:3144615 | T | C | 1 | a0002c0006 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.513T>C | p.Asn171Asn | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/8 | 591/2252 | 513/1305 | 171/434 | chr3 | 3144615 | |||
| chr3:3146601 | T | C | 1 | a0001c0010 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.780T>C | p.Asp260Asp | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/8 | 858/2252 | 780/1305 | 260/434 | chr3 | 3146601 | |||
| chr3:3147592 | C | T | 1 | a0002c0008 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.945C>T | p.Ile315Ile | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/8 | 1023/2252 | 945/1305 | 315/434 | chr3 | 3147592 | |||
| chr3:3147595 | A | G | 7 | a0001c0001 a0001c0010 a0002c0005 others(4): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
synonymous_variant | LOW | c.948A>G | p.Ala316Ala | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/8 | 1026/2252 | 948/1305 | 316/434 | chr3 | 3147595 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3126942 | C | A | 3 | a0001c0004t0008 a0001c0004t0016 a0003c0014t0016 |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-76C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/8 | 2099 | chr3 | 3126942 | ||||||
| chr3:3148206 | C | T | 1 | a0004c0013t0026 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*52C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 52 | chr3 | 3148206 | ||||||
| chr3:3148275 | A | C | 1 | a0001c0001t0025 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*121A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 121 | chr3 | 3148275 | ||||||
| chr3:3148365 | T | C | 1 | a0001c0001t0018 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*211T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 211 | chr3 | 3148365 | ||||||
| chr3:3148403 | C | G | 1 | a0001c0001t0012 | 4 | NA18944.hp1 NA18967.hp2 NA19060.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*249C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 249 | chr3 | 3148403 | ||||||
| chr3:3148463 | C | T | 1 | a0001c0001t0024 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 309 | chr3 | 3148463 | ||||||
| chr3:3148556 | T | C | 7 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0019 others(4): Show |
56 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*402T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 402 | chr3 | 3148556 | ||||||
| chr3:3148564 | G | C | 1 | a0001c0001t0011 | 4 | NA18612.hp2 NA18969.hp2 NA18990.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*410G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 410 | chr3 | 3148564 | ||||||
| chr3:3148594 | C | T | 2 | a0001c0001t0018 a0001c0004t0008 |
6 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*440C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 440 | chr3 | 3148594 | ||||||
| chr3:3148622 | A | G | 1 | a0002c0003t0023 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 468 | chr3 | 3148622 | ||||||
| chr3:3148639 | T | C | 1 | a0001c0001t0013 | 3 | HG01891.hp2 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*485T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 485 | chr3 | 3148639 | ||||||
| chr3:3148642 | G | A | 1 | a0001c0001t0017 | 2 | HG01106.hp2 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*488G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 488 | chr3 | 3148642 | ||||||
| chr3:3148767 | G | A | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(26): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
3_prime_UTR_variant | MODIFIER | c.*613G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 613 | chr3 | 3148767 | ||||||
| chr3:3148793 | A | G | 1 | a0001c0002t0020 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 639 | chr3 | 3148793 | ||||||
| chr3:3148804 | T | TATTA | 7 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(4): Show |
100 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*659_*662dupATTA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 663 | INFO_REALIGN_3_PRIME | chr3 | 3148804 | |||||
| chr3:3148815 | T | TA | 3 | a0001c0001t0005 a0002c0005t0010 a0002c0006t0010 |
23 | HG00738.hp2 HG01071.hp2 HG01081.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*662dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 663 | INFO_REALIGN_3_PRIME | chr3 | 3148815 | |||||
| chr3:3148817 | T | C | 1 | a0001c0001t0021 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*663T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 663 | chr3 | 3148817 | ||||||
| chr3:3148874 | A | G | 1 | a0001c0001t0022 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 720 | chr3 | 3148874 | ||||||
| chr3:3148898 | C | T | 1 | a0002c0003t0015 | 3 | HG02965.hp2 HG02976.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*744C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 744 | chr3 | 3148898 | ||||||
| chr3:3148952 | C | CTATT | 1 | a0001c0001t0009 | 5 | HG02818.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*802dupTATT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 803 | INFO_REALIGN_3_PRIME | chr3 | 3148952 | |||||
| chr3:3148962 | A | ATATTCTC others(12): Show |
4 | a0001c0001t0005 a0001c0001t0007 a0002c0005t0010 others(1): Show |
30 | HG00738.hp2 HG01071.hp1 HG01071.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*821_*822insAAGATT others(13): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 822 | INFO_REALIGN_3_PRIME | chr3 | 3148962 | |||||
| chr3:3148962 | A | ATATTCTC others(8): Show |
9 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(6): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*810_*824dupATTCTC others(9): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 825 | INFO_REALIGN_3_PRIME | chr3 | 3148962 | |||||
| chr3:3148970 | T | TAAAG | 3 | a0001c0002t0019 a0001c0004t0016 a0003c0014t0016 |
3 | HG00642.hp2 HG02622.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*818_*821dupAAGA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 822 | INFO_REALIGN_3_PRIME | chr3 | 3148970 | |||||
| chr3:3148970 | T | TAAAGATT others(12): Show |
7 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0021 others(4): Show |
172 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*824_*825insATTCTC others(13): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 825 | INFO_REALIGN_3_PRIME | chr3 | 3148970 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3127088 | C | A | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+98C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127088 | |||||||
| chr3:3127166 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-28+176C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127166 | |||||||
| chr3:3127207 | C | T | 1 | a0001c0001t0006g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-28+217C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127207 | |||||||
| chr3:3127210 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-28+220C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127210 | |||||||
| chr3:3127238 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-28+248G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127238 | |||||||
| chr3:3127273 | A | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+283A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127273 | |||||||
| chr3:3127287 | G | C | 2 | a0001c0002t0003g0002 a0001c0002t0020g0002 |
6 | HG00438.hp1 HG02155.hp2 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+297G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127287 | |||||||
| chr3:3127354 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+364G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127354 | |||||||
| chr3:3127357 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+367G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127357 | |||||||
| chr3:3127360 | A | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+370A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127360 | |||||||
| chr3:3127369 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+379G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127369 | |||||||
| chr3:3127370 | T | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+380T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127370 | |||||||
| chr3:3127377 | G | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+387G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127377 | |||||||
| chr3:3127381 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+391C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127381 | |||||||
| chr3:3127384 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+394G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127384 | |||||||
| chr3:3127386 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+396G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127386 | |||||||
| chr3:3127387 | G | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+397G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127387 | |||||||
| chr3:3127389 | C | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+399C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127389 | |||||||
| chr3:3127391 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+401G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127391 | |||||||
| chr3:3127394 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+404G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127394 | |||||||
| chr3:3127395 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+405G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127395 | |||||||
| chr3:3127396 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+406G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127396 | |||||||
| chr3:3127399 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+409G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127399 | |||||||
| chr3:3127400 | C | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+410C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127400 | |||||||
| chr3:3127493 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-28+503G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127493 | |||||||
| chr3:3127506 | A | T | 68 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0122 others(65): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-28+516A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127506 | |||||||
| chr3:3127508 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+518G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127508 | |||||||
| chr3:3127534 | A | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+544A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127534 | |||||||
| chr3:3127589 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+599G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127589 | |||||||
| chr3:3127590 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+600A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127590 | |||||||
| chr3:3127602 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+612G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127602 | |||||||
| chr3:3127605 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+615G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127605 | |||||||
| chr3:3127606 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+616G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127606 | |||||||
| chr3:3127619 | A | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+629A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127619 | |||||||
| chr3:3127620 | T | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+630T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127620 | |||||||
| chr3:3127622 | C | A | 2 | a0001c0002t0003g0002 a0001c0002t0003g0042 |
5 | HG01168.hp2 HG01169.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+632C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127622 | |||||||
| chr3:3127633 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+643A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127633 | |||||||
| chr3:3127634 | C | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+644C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127634 | |||||||
| chr3:3127635 | A | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+645A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127635 | |||||||
| chr3:3127650 | T | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+660T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127650 | |||||||
| chr3:3127651 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+661C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127651 | |||||||
| chr3:3127677 | GGTGGGGA others(26): Show |
G | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+688_-28+720del others(33): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127677 | |||||||
| chr3:3127690 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-28+700G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127690 | |||||||
| chr3:3127713 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+723A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127713 | |||||||
| chr3:3127714 | C | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+724C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127714 | |||||||
| chr3:3127719 | T | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+729T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127719 | |||||||
| chr3:3127720 | T | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0006g0024 others(5): Show |
9 | HG00280.hp1 HG01106.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+730T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127720 | |||||||
| chr3:3127733 | A | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+743A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127733 | |||||||
| chr3:3127734 | C | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+744C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127734 | |||||||
| chr3:3127738 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+748G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127738 | |||||||
| chr3:3127739 | T | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-28+749T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127739 | |||||||
| chr3:3127739 | T | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+749T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127739 | |||||||
| chr3:3127753 | A | ACCCAGCA others(15): Show |
1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+766_-28+767ins others(22): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3127753 | ||||||
| chr3:3127776 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-28+786C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127776 | |||||||
| chr3:3127782 | C | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0002t0003g0002 others(16): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-28+792C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127782 | |||||||
| chr3:3127811 | A | C | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+821A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127811 | |||||||
| chr3:3127812 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+822C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127812 | |||||||
| chr3:3127923 | A | C | 1 | a0001c0001t0002g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-28+933A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127923 | |||||||
| chr3:3127953 | G | T | 2 | a0002c0005t0010g0019 a0002c0006t0010g0019 |
4 | HG03130.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+963G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127953 | |||||||
| chr3:3128049 | T | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0054 a0001c0001t0005g0055 others(1): Show |
5 | HG03491.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-965T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128049 | |||||||
| chr3:3128056 | A | G | 1 | a0001c0001t0005g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-27-958A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128056 | |||||||
| chr3:3128235 | C | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-27-779C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128235 | |||||||
| chr3:3128255 | C | T | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-27-759C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128255 | |||||||
| chr3:3128368 | G | A | 5 | a0001c0001t0001g0057 a0001c0004t0008g0023 a0001c0004t0008g0044 others(2): Show |
6 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-646G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128368 | |||||||
| chr3:3128394 | C | G | 18 | a0001c0001t0005g0147 a0001c0002t0003g0002 a0001c0002t0003g0011 others(15): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-27-620C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128394 | |||||||
| chr3:3128410 | A | G | 1 | a0001c0001t0002g0040 | 2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-27-604A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128410 | |||||||
| chr3:3128481 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-27-533C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128481 | |||||||
| chr3:3128500 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-27-514G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128500 | |||||||
| chr3:3128547 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-27-467T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128547 | |||||||
| chr3:3128598 | C | CA | 24 | a0001c0001t0002g0022 a0001c0001t0002g0035 a0001c0001t0002g0123 others(21): Show |
61 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-27-393dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | ||||||
| chr3:3128598 | C | CAA | 42 | a0001c0001t0001g0122 a0001c0001t0002g0005 a0001c0001t0002g0012 others(39): Show |
75 | HG00408.hp2 HG00621.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-27-394_-27-393dup others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | ||||||
| chr3:3128598 | C | CAAA | 19 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0099 others(16): Show |
22 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-27-395_-27-393dup others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | ||||||
| chr3:3128598 | C | CAAAA | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(39): Show |
139 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-27-396_-27-393dup others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | ||||||
| chr3:3128598 | C | CAAAAA | 15 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0059 others(12): Show |
30 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.-27-397_-27-393dup others(5): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | ||||||
| chr3:3128598 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0005g0130 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-27-404_-27-393del others(12): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | ||||||
| chr3:3128598 | CAAAAAAA others(6): Show |
C | 10 | a0001c0001t0002g0007 a0001c0001t0002g0037 a0001c0001t0002g0038 others(7): Show |
23 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.-27-405_-27-393del others(13): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | ||||||
| chr3:3128613 | A | AAAG | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-399_-27-398ins others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128613 | ||||||
| chr3:3128725 | G | C | 68 | a0001c0001t0001g0122 a0001c0001t0002g0005 a0001c0001t0002g0007 others(65): Show |
118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-27-289G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128725 | |||||||
| chr3:3128776 | A | AGTT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.-27-237_-27-235dup others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128776 | ||||||
| chr3:3128783 | G | A | 1 | a0002c0003t0004g0157 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-27-231G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128783 | |||||||
| chr3:3128845 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-27-169A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128845 | |||||||
| chr3:3129226 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.148+38A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129226 | |||||||
| chr3:3129282 | T | C | 18 | a0001c0001t0005g0147 a0001c0002t0003g0002 a0001c0002t0003g0011 others(15): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.148+94T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129282 | |||||||
| chr3:3129321 | G | A | 3 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0123 |
3 | HG02559.hp1 HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.148+133G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129321 | |||||||
| chr3:3129338 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(56): Show |
172 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.148+150C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129338 | |||||||
| chr3:3129339 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.148+151A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129339 | |||||||
| chr3:3129361 | G | C | 1 | a0001c0001t0002g0105 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.148+173G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129361 | |||||||
| chr3:3129425 | G | C | 1 | a0001c0004t0008g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.148+237G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129425 | |||||||
| chr3:3129441 | G | A | 68 | a0001c0001t0001g0122 a0001c0001t0002g0005 a0001c0001t0002g0007 others(65): Show |
118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.148+253G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129441 | |||||||
| chr3:3129587 | A | C | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+399A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129587 | |||||||
| chr3:3129587 | A | G | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.148+399A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129587 | |||||||
| chr3:3129602 | TAAAAG | T | 2 | a0001c0001t0009g0021 a0001c0001t0009g0034 |
5 | HG02818.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+416_148+420del others(5): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3129602 | ||||||
| chr3:3129705 | T | C | 3 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0001c0001t0006g0048 |
4 | HG00280.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+517T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129705 | |||||||
| chr3:3129742 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.148+554C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129742 | |||||||
| chr3:3129754 | G | C | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.148+566G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129754 | |||||||
| chr3:3129776 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.148+588C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129776 | |||||||
| chr3:3129816 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148+628T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129816 | |||||||
| chr3:3129818 | C | A | 67 | a0001c0001t0001g0059 a0001c0001t0002g0005 a0001c0001t0002g0007 others(64): Show |
117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.148+630C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129818 | |||||||
| chr3:3129848 | C | G | 1 | a0004c0013t0026g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.148+660C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129848 | |||||||
| chr3:3129895 | C | T | 1 | a0004c0013t0026g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.148+707C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129895 | |||||||
| chr3:3129975 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG00558.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.148+787G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129975 | |||||||
| chr3:3130002 | G | A | 1 | a0001c0002t0003g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.148+814G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130002 | |||||||
| chr3:3130029 | G | GCCTGACT | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.148+843_148+844ins others(7): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3130029 | ||||||
| chr3:3130203 | A | G | 1 | a0001c0001t0022g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.148+1015A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130203 | |||||||
| chr3:3130213 | T | C | 21 | a0001c0001t0002g0107 a0001c0001t0003g0163 a0001c0001t0005g0147 others(18): Show |
56 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.148+1025T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130213 | |||||||
| chr3:3130213 | T | G | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+1025T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130213 | |||||||
| chr3:3130289 | T | C | 1 | a0002c0003t0004g0157 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.148+1101T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130289 | |||||||
| chr3:3130332 | A | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(44): Show |
154 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.148+1144A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130332 | |||||||
| chr3:3130439 | C | T | 1 | a0004c0013t0026g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.148+1251C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130439 | |||||||
| chr3:3130502 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.148+1314G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130502 | |||||||
| chr3:3130513 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.148+1325A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130513 | |||||||
| chr3:3130620 | T | C | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.148+1432T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130620 | |||||||
| chr3:3130711 | C | T | 3 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0001c0001t0006g0048 |
4 | HG00280.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+1523C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130711 | |||||||
| chr3:3130752 | T | G | 3 | a0001c0004t0016g0152 a0001c0012t0003g0153 a0003c0014t0016g0151 |
3 | HG00642.hp2 HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.148+1564T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130752 | |||||||
| chr3:3130759 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0017g0051 others(2): Show |
5 | HG01106.hp2 HG01175.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+1571G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130759 | |||||||
| chr3:3130899 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(52): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148+1711C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130899 | |||||||
| chr3:3130901 | G | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(52): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148+1713G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130901 | |||||||
| chr3:3130915 | C | G | 4 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0001c0001t0006g0048 others(1): Show |
5 | HG00280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+1727C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130915 | |||||||
| chr3:3130952 | T | G | 1 | a0001c0001t0001g0062 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.148+1764T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130952 | |||||||
| chr3:3131009 | G | GA | 3 | a0001c0001t0002g0165 a0001c0001t0012g0020 a0001c0001t0012g0108 |
5 | NA18943.hp2 NA18944.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+1822dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3131009 | ||||||
| chr3:3131065 | A | G | 1 | a0001c0002t0003g0148 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.148+1877A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131065 | |||||||
| chr3:3131077 | T | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+1889T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131077 | |||||||
| chr3:3131077 | TA | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0089 others(8): Show |
12 | HG00738.hp1 HG00741.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.148+1904delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3131077 | ||||||
| chr3:3131176 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.148+1988C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131176 | |||||||
| chr3:3131236 | C | T | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+2048C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131236 | |||||||
| chr3:3131272 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(53): Show |
167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.148+2084T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131272 | |||||||
| chr3:3131296 | A | G | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+2108A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131296 | |||||||
| chr3:3131313 | G | C | 1 | a0001c0002t0003g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.148+2125G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131313 | |||||||
| chr3:3131332 | A | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(58): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.148+2144A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131332 | |||||||
| chr3:3131398 | T | A | 1 | a0001c0001t0025g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.148+2210T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131398 | |||||||
| chr3:3131413 | A | G | 3 | a0001c0001t0007g0032 a0001c0001t0007g0068 a0001c0001t0007g0097 |
4 | HG02109.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+2225A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131413 | |||||||
| chr3:3131414 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.148+2226T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131414 | |||||||
| chr3:3131428 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0124 |
2 | HG02135.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.148+2240T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131428 | |||||||
| chr3:3131463 | AAACTGGC others(2196): Show |
A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+2276_149-3594d others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131463 | |||||||
| chr3:3131505 | C | T | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+2317C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131505 | |||||||
| chr3:3131544 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.148+2356A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131544 | |||||||
| chr3:3131554 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.148+2366G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131554 | |||||||
| chr3:3131669 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.148+2481G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131669 | |||||||
| chr3:3131839 | AAAAC | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0017g0051 others(1): Show |
4 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+2658_148+2661d others(6): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3131839 | ||||||
| chr3:3131841 | A | G | 1 | a0001c0001t0002g0124 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.148+2653A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131841 | |||||||
| chr3:3131892 | A | G | 1 | a0001c0001t0018g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.148+2704A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131892 | |||||||
| chr3:3131965 | A | G | 71 | a0001c0001t0001g0059 a0001c0001t0002g0005 a0001c0001t0002g0007 others(68): Show |
123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.148+2777A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131965 | |||||||
| chr3:3132007 | G | A | 1 | a0001c0001t0002g0005 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.148+2819G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132007 | |||||||
| chr3:3132122 | G | A | 5 | a0001c0001t0005g0010 a0001c0001t0005g0025 a0001c0001t0005g0054 others(2): Show |
5 | HG02602.hp1 HG03491.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+2934G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132122 | |||||||
| chr3:3132168 | C | T | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.148+2980C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132168 | |||||||
| chr3:3132222 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.148+3034G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132222 | |||||||
| chr3:3132233 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.148+3045G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132233 | |||||||
| chr3:3132252 | A | G | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.148+3064A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132252 | |||||||
| chr3:3132345 | T | C | 1 | a0001c0002t0019g0002 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.148+3157T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132345 | |||||||
| chr3:3132425 | C | T | 1 | a0001c0001t0002g0007 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.148+3237C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132425 | |||||||
| chr3:3132426 | G | A | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+3238G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132426 | |||||||
| chr3:3132519 | CTG | C | 67 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(64): Show |
117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.148+3332_148+3333d others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132519 | |||||||
| chr3:3132546 | G | A | 18 | a0001c0001t0005g0147 a0001c0002t0003g0002 a0001c0002t0003g0011 others(15): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.148+3358G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132546 | |||||||
| chr3:3132589 | A | G | 2 | a0001c0002t0003g0002 a0001c0002t0003g0042 |
5 | HG01168.hp2 HG01169.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+3401A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132589 | |||||||
| chr3:3132590 | C | A | 2 | a0001c0002t0003g0002 a0001c0002t0003g0042 |
5 | HG01168.hp2 HG01169.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+3402C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132590 | |||||||
| chr3:3132614 | A | G | 1 | a0001c0001t0001g0006 | 2 | NA18970.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.148+3426A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132614 | |||||||
| chr3:3132623 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.148+3435G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132623 | |||||||
| chr3:3132625 | A | G | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3437A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132625 | |||||||
| chr3:3132632 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(2): Show |
21 | HG00741.hp1 HG01069.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.148+3444T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132632 | |||||||
| chr3:3132682 | TA | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(147): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.148+3507delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132682 | ||||||
| chr3:3132687 | AAAAAAAA others(3): Show |
A | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3507_148+3516d others(12): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132687 | ||||||
| chr3:3132697 | T | A | 5 | a0001c0001t0001g0006 a0001c0002t0003g0002 a0001c0002t0003g0011 others(2): Show |
12 | HG00597.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.148+3509T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132697 | |||||||
| chr3:3132704 | A | T | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3516A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132704 | |||||||
| chr3:3132714 | A | C | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+3526A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132714 | |||||||
| chr3:3132731 | G | GA | 37 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0131 others(34): Show |
88 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.148+3556dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132731 | ||||||
| chr3:3132737 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.148+3557_148+3566d others(12): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132737 | ||||||
| chr3:3132740 | A | C | 1 | a0001c0001t0018g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.148+3552A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132740 | |||||||
| chr3:3132741 | A | C | 2 | a0001c0001t0006g0047 a0001c0001t0006g0048 |
2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.148+3553A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132741 | |||||||
| chr3:3132743 | AAC | A | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3559_148+3560d others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132743 | ||||||
| chr3:3132745 | C | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(150): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.148+3557C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132745 | |||||||
| chr3:3132746 | A | AAC | 6 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0050 others(3): Show |
6 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+3558_148+3559i others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132746 | |||||||
| chr3:3132746 | A | C | 1 | a0001c0001t0001g0004 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.148+3558A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132746 | |||||||
| chr3:3132747 | C | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(4): Show |
7 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+3559C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132747 | |||||||
| chr3:3132747 | C | CA | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(57): Show |
169 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.148+3569dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132747 | ||||||
| chr3:3132749 | A | C | 1 | a0002c0003t0004g0003 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.148+3561A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132749 | |||||||
| chr3:3132758 | C | A | 25 | a0001c0001t0003g0163 a0001c0002t0003g0002 a0001c0002t0003g0011 others(22): Show |
61 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.148+3570C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132758 | |||||||
| chr3:3132805 | G | C | 1 | a0001c0001t0025g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.148+3617G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132805 | |||||||
| chr3:3132837 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG00741.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.148+3649T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132837 | |||||||
| chr3:3133043 | C | G | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.148+3855C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133043 | |||||||
| chr3:3133081 | C | G | 1 | a0001c0001t0001g0008 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.148+3893C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133081 | |||||||
| chr3:3133137 | G | A | 1 | a0002c0003t0004g0003 | 3 | HG02257.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.148+3949G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133137 | |||||||
| chr3:3133163 | T | G | 1 | a0001c0002t0003g0002 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.148+3975T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133163 | |||||||
| chr3:3133232 | G | T | 2 | a0001c0001t0017g0051 a0001c0001t0017g0052 |
2 | HG01106.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.149-4028G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133232 | |||||||
| chr3:3133271 | G | C | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-3989G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133271 | |||||||
| chr3:3133279 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.149-3981T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133279 | |||||||
| chr3:3133349 | T | A | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-3911T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133349 | |||||||
| chr3:3133377 | A | C | 1 | a0001c0001t0025g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.149-3883A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133377 | |||||||
| chr3:3133417 | G | T | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-3843G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133417 | |||||||
| chr3:3133422 | A | G | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-3838A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133422 | |||||||
| chr3:3133490 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.149-3770G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133490 | |||||||
| chr3:3133523 | A | C | 1 | a0003c0014t0016g0151 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.149-3737A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133523 | |||||||
| chr3:3133555 | C | CA | 7 | a0001c0001t0001g0006 a0001c0004t0008g0023 a0001c0004t0008g0044 others(4): Show |
8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.149-3692dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3133555 | ||||||
| chr3:3133569 | T | A | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-3691T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133569 | |||||||
| chr3:3133576 | C | T | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-3684C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133576 | |||||||
| chr3:3133588 | C | G | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-3672C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133588 | |||||||
| chr3:3133665 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.149-3595G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133665 | |||||||
| chr3:3133669 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3591A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133669 | |||||||
| chr3:3133670 | GT | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3589delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133670 | |||||||
| chr3:3133673 | C | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3587C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133673 | |||||||
| chr3:3133677 | G | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3583G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133677 | |||||||
| chr3:3133678 | G | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3582G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133678 | |||||||
| chr3:3133682 | T | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3578T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133682 | |||||||
| chr3:3133685 | T | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3575T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133685 | |||||||
| chr3:3133688 | ACAG | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3571_149-3569d others(5): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133688 | |||||||
| chr3:3133693 | G | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3567G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133693 | |||||||
| chr3:3133695 | G | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3565G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133695 | |||||||
| chr3:3133699 | T | TG | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3561_149-3560i others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133699 | |||||||
| chr3:3133702 | CGCTCAGT others(444): Show |
C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3557_149-3107d others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133702 | |||||||
| chr3:3133708 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-3552G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133708 | |||||||
| chr3:3133720 | G | A | 1 | a0001c0004t0008g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.149-3540G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133720 | |||||||
| chr3:3133786 | G | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0120 |
3 | NA18973.hp1 NA18993.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.149-3474G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133786 | |||||||
| chr3:3133917 | C | T | 2 | a0001c0002t0003g0002 a0001c0002t0020g0002 |
5 | HG00438.hp1 HG02155.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-3343C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133917 | |||||||
| chr3:3133922 | A | G | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-3338A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133922 | |||||||
| chr3:3134063 | G | C | 1 | a0001c0001t0001g0001 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.149-3197G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134063 | |||||||
| chr3:3134090 | T | G | 2 | a0001c0002t0014g0039 a0005c0007t0014g0138 |
3 | HG02109.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.149-3170T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134090 | |||||||
| chr3:3134131 | A | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0120 |
3 | NA18973.hp1 NA18993.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.149-3129A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134131 | |||||||
| chr3:3134157 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3103A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134157 | |||||||
| chr3:3134163 | T | TG | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3097_149-3096i others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134163 | |||||||
| chr3:3134166 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3094A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134166 | |||||||
| chr3:3134167 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3093A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134167 | |||||||
| chr3:3134169 | G | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3091G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134169 | |||||||
| chr3:3134171 | A | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3089A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134171 | |||||||
| chr3:3134174 | T | TG | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3086_149-3085i others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134174 | |||||||
| chr3:3134176 | G | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3084G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134176 | |||||||
| chr3:3134177 | C | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3083C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134177 | |||||||
| chr3:3134180 | A | ATGTC | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3080_149-3079i others(6): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134180 | |||||||
| chr3:3134181 | G | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3079G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134181 | |||||||
| chr3:3134187 | T | G | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-3073T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134187 | |||||||
| chr3:3134190 | A | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3070A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134190 | |||||||
| chr3:3134192 | T | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3068T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134192 | |||||||
| chr3:3134192 | T | C | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-3068T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134192 | |||||||
| chr3:3134193 | GT | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3065delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3134193 | ||||||
| chr3:3134197 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3063A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134197 | |||||||
| chr3:3134200 | GCC | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3059_149-3058d others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134200 | |||||||
| chr3:3134204 | C | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3056C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134204 | |||||||
| chr3:3134206 | C | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3054C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134206 | |||||||
| chr3:3134208 | GT | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3049delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3134208 | ||||||
| chr3:3134211 | T | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3049T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134211 | |||||||
| chr3:3134214 | GT | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3045delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134214 | |||||||
| chr3:3134216 | A | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3044A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134216 | |||||||
| chr3:3134218 | G | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3042G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134218 | |||||||
| chr3:3134219 | A | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3041A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134219 | |||||||
| chr3:3134225 | GATATCAG others(3): Show |
G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3034_149-3025d others(12): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134225 | |||||||
| chr3:3134238 | G | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3022G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134238 | |||||||
| chr3:3134241 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3019A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134241 | |||||||
| chr3:3134242 | T | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3018T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134242 | |||||||
| chr3:3134248 | AATCTTGA others(27): Show |
A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3011_149-2978d others(36): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134248 | |||||||
| chr3:3134286 | T | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2974T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134286 | |||||||
| chr3:3134287 | GT | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2972delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134287 | |||||||
| chr3:3134292 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2968A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134292 | |||||||
| chr3:3134294 | T | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2966T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134294 | |||||||
| chr3:3134295 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2965A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134295 | |||||||
| chr3:3134297 | G | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2963G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134297 | |||||||
| chr3:3134298 | C | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2962C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134298 | |||||||
| chr3:3134306 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2954A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134306 | |||||||
| chr3:3134308 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2952A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134308 | |||||||
| chr3:3134309 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2951A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134309 | |||||||
| chr3:3134315 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2945A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134315 | |||||||
| chr3:3134318 | ACTGCTCT others(1118): Show |
A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2941_149-1817d others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134318 | |||||||
| chr3:3134343 | G | A | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-2917G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134343 | |||||||
| chr3:3134353 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.149-2907G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134353 | |||||||
| chr3:3134402 | G | T | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-2858G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134402 | |||||||
| chr3:3134617 | C | T | 70 | a0001c0001t0001g0059 a0001c0001t0002g0005 a0001c0001t0002g0007 others(67): Show |
120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.149-2643C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134617 | |||||||
| chr3:3134694 | A | G | 1 | a0001c0002t0003g0011 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149-2566A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134694 | |||||||
| chr3:3134729 | T | C | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-2531T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134729 | |||||||
| chr3:3134825 | A | G | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.149-2435A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134825 | |||||||
| chr3:3134864 | T | A | 2 | a0001c0001t0003g0163 a0001c0012t0003g0153 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-2396T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134864 | |||||||
| chr3:3134943 | G | T | 1 | a0001c0001t0002g0007 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.149-2317G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134943 | |||||||
| chr3:3134962 | T | A | 7 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(4): Show |
8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.149-2298T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134962 | |||||||
| chr3:3135037 | AAGAG | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0006 |
4 | HG02055.hp1 HG02486.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-2219_149-2216d others(6): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3135037 | ||||||
| chr3:3135253 | G | A | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-2007G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135253 | |||||||
| chr3:3135415 | C | G | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-1845C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135415 | |||||||
| chr3:3135431 | C | T | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-1829C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135431 | |||||||
| chr3:3135435 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.149-1825T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135435 | |||||||
| chr3:3135445 | G | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1815G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135445 | |||||||
| chr3:3135451 | G | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1809G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135451 | |||||||
| chr3:3135454 | G | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1806G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135454 | |||||||
| chr3:3135456 | A | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1804A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135456 | |||||||
| chr3:3135457 | T | TCTGTCG | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1803_149-1802i others(8): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135457 | |||||||
| chr3:3135458 | T | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1802T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135458 | |||||||
| chr3:3135460 | A | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1800A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135460 | |||||||
| chr3:3135464 | G | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1796G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135464 | |||||||
| chr3:3135465 | A | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1795A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135465 | |||||||
| chr3:3135468 | T | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1792T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135468 | |||||||
| chr3:3135469 | GA | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1790delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135469 | |||||||
| chr3:3135473 | T | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1787T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135473 | |||||||
| chr3:3135474 | G | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1786G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135474 | |||||||
| chr3:3135480 | A | G | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-1780A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135480 | |||||||
| chr3:3135493 | C | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.149-1767C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135493 | |||||||
| chr3:3135536 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-1724G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135536 | |||||||
| chr3:3135778 | C | T | 1 | a0001c0001t0005g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.149-1482C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135778 | |||||||
| chr3:3135790 | T | C | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-1470T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135790 | |||||||
| chr3:3135872 | G | C | 1 | a0001c0001t0007g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.149-1388G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135872 | |||||||
| chr3:3135899 | C | T | 2 | a0001c0001t0002g0118 a0001c0001t0002g0126 |
2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.149-1361C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135899 | |||||||
| chr3:3135967 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0155 |
2 | HG01993.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.149-1293A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135967 | |||||||
| chr3:3135991 | C | T | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-1269C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135991 | |||||||
| chr3:3136018 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149-1242G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136018 | |||||||
| chr3:3136151 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(51): Show |
165 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.149-1109C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136151 | |||||||
| chr3:3136207 | T | C | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-1053T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136207 | |||||||
| chr3:3136238 | A | T | 7 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(4): Show |
8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.149-1022A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136238 | |||||||
| chr3:3136248 | A | T | 8 | a0001c0001t0003g0163 a0001c0004t0008g0023 a0001c0004t0008g0044 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-1012A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136248 | |||||||
| chr3:3136289 | T | G | 17 | a0001c0002t0003g0002 a0001c0002t0003g0011 a0001c0002t0003g0014 others(14): Show |
52 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.149-971T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136289 | |||||||
| chr3:3136293 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.149-967T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136293 | |||||||
| chr3:3136304 | C | G | 1 | a0001c0001t0001g0036 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.149-956C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136304 | |||||||
| chr3:3136363 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0017g0051 others(1): Show |
4 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-897A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136363 | |||||||
| chr3:3136421 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.149-839A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136421 | |||||||
| chr3:3136424 | G | A | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.149-836G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136424 | |||||||
| chr3:3136426 | A | T | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-834A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136426 | |||||||
| chr3:3136506 | T | A | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-754T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136506 | |||||||
| chr3:3136638 | G | A | 92 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(89): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.149-622G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136638 | |||||||
| chr3:3136644 | CTTTCTTT others(3): Show |
C | 1 | a0002c0003t0004g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149-602_149-593del others(10): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3136644 | ||||||
| chr3:3136658 | CT | C | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0029 others(32): Show |
66 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.149-588delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3136658 | ||||||
| chr3:3136874 | C | G | 2 | a0001c0001t0002g0134 a0001c0001t0002g0135 |
2 | HG00323.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.149-386C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136874 | |||||||
| chr3:3136942 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.149-318C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136942 | |||||||
| chr3:3137080 | C | T | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.149-180C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3137080 | |||||||
| chr3:3137089 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149-171A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3137089 | |||||||
| chr3:3137239 | T | C | 1 | a0001c0001t0006g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.149-21T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3137239 | |||||||
| chr3:3137241 | T | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0100 |
2 | NA18973.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.149-19T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3137241 | |||||||
| chr3:3137547 | A | G | 1 | a0001c0001t0009g0021 | 3 | HG03098.hp2 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.342+94A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137547 | |||||||
| chr3:3137578 | A | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.342+125A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137578 | |||||||
| chr3:3137629 | C | T | 1 | a0001c0002t0003g0146 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.342+176C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137629 | |||||||
| chr3:3137682 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0101 |
2 | HG03017.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.342+229T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137682 | |||||||
| chr3:3137684 | A | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+231A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137684 | |||||||
| chr3:3137685 | C | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+232C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137685 | |||||||
| chr3:3137687 | A | T | 7 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(4): Show |
8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+234A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137687 | |||||||
| chr3:3137698 | A | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+245A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137698 | |||||||
| chr3:3137699 | A | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+246A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137699 | |||||||
| chr3:3137700 | G | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+247G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137700 | |||||||
| chr3:3137701 | A | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+248A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137701 | |||||||
| chr3:3137703 | G | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+250G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137703 | |||||||
| chr3:3137705 | G | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+252G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137705 | |||||||
| chr3:3137708 | A | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+255A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137708 | |||||||
| chr3:3137709 | C | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+256C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137709 | |||||||
| chr3:3137710 | G | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+257G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137710 | |||||||
| chr3:3137712 | A | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+259A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137712 | |||||||
| chr3:3137715 | G | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+262G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137715 | |||||||
| chr3:3137716 | A | G | 18 | a0001c0001t0005g0147 a0001c0002t0003g0002 a0001c0002t0003g0011 others(15): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.342+263A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137716 | |||||||
| chr3:3137716 | A | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+263A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137716 | |||||||
| chr3:3137717 | C | T | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+264C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137717 | |||||||
| chr3:3137720 | T | TGAGACGG others(269): Show |
1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+267_342+268ins others(276): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137720 | |||||||
| chr3:3137723 | A | G | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+270A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137723 | |||||||
| chr3:3137724 | T | G | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+271T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137724 | |||||||
| chr3:3137725 | A | C | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+272A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137725 | |||||||
| chr3:3137726 | A | C | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+273A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137726 | |||||||
| chr3:3137901 | C | T | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+448C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137901 | |||||||
| chr3:3138231 | G | T | 1 | a0001c0001t0002g0133 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.342+778G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138231 | |||||||
| chr3:3138235 | G | C | 1 | a0004c0013t0026g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.342+782G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138235 | |||||||
| chr3:3138257 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.342+804C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138257 | |||||||
| chr3:3138373 | G | T | 67 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(64): Show |
117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.342+920G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138373 | |||||||
| chr3:3138489 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
177 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.342+1036C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138489 | |||||||
| chr3:3138607 | C | T | 1 | a0001c0001t0005g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.342+1154C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138607 | |||||||
| chr3:3138679 | C | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0120 |
3 | NA18973.hp1 NA18993.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.342+1226C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138679 | |||||||
| chr3:3138768 | G | A | 6 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(3): Show |
7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+1315G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138768 | |||||||
| chr3:3138991 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.343-1519G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138991 | |||||||
| chr3:3139022 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(62): Show |
178 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.343-1488T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139022 | |||||||
| chr3:3139079 | A | G | 1 | a0001c0001t0006g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.343-1431A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139079 | |||||||
| chr3:3139178 | A | C | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.343-1332A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139178 | |||||||
| chr3:3139252 | G | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.343-1258G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139252 | |||||||
| chr3:3139556 | G | T | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.343-954G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139556 | |||||||
| chr3:3139613 | A | G | 73 | a0001c0001t0001g0059 a0001c0001t0001g0122 a0001c0001t0002g0005 others(70): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.343-897A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139613 | |||||||
| chr3:3139629 | T | C | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.343-881T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139629 | |||||||
| chr3:3139647 | G | A | 1 | a0004c0013t0026g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.343-863G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139647 | |||||||
| chr3:3139656 | A | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.343-854A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139656 | |||||||
| chr3:3139658 | A | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-852A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139658 | |||||||
| chr3:3139671 | G | C | 7 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(4): Show |
8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-839G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139671 | |||||||
| chr3:3139687 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.343-823G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139687 | |||||||
| chr3:3139716 | T | C | 25 | a0001c0001t0003g0163 a0001c0002t0003g0002 a0001c0002t0003g0011 others(22): Show |
61 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.343-794T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139716 | |||||||
| chr3:3139735 | C | A | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.343-775C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139735 | |||||||
| chr3:3140072 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.343-438G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140072 | |||||||
| chr3:3140091 | T | C | 1 | a0002c0003t0004g0043 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.343-419T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140091 | |||||||
| chr3:3140107 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.343-403C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140107 | |||||||
| chr3:3140119 | A | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.343-391A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140119 | |||||||
| chr3:3140295 | T | TA | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.343-215_343-214ins others(1): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140295 | |||||||
| chr3:3140296 | T | A | 2 | a0001c0001t0001g0078 a0002c0003t0004g0043 |
3 | HG02055.hp2 HG02970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.343-214T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140296 | |||||||
| chr3:3140303 | A | T | 19 | a0001c0001t0001g0050 a0001c0001t0002g0005 a0001c0002t0003g0002 others(16): Show |
54 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.343-207A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140303 | |||||||
| chr3:3140304 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.343-206A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140304 | |||||||
| chr3:3140364 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG00099.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.343-146A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140364 | |||||||
| chr3:3140392 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.343-118A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140392 | |||||||
| chr3:3140741 | A | G | 2 | a0001c0002t0014g0039 a0005c0007t0014g0138 |
3 | HG02109.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.481+93A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3140741 | |||||||
| chr3:3140801 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.481+153A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3140801 | |||||||
| chr3:3140805 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0064 |
5 | HG02080.hp2 NA18998.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+157G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3140805 | |||||||
| chr3:3141040 | C | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0120 |
3 | NA18973.hp1 NA18993.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.481+392C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141040 | |||||||
| chr3:3141111 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.481+463T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141111 | |||||||
| chr3:3141180 | C | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.481+532C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141180 | |||||||
| chr3:3141216 | C | G | 2 | a0001c0001t0002g0118 a0001c0001t0002g0126 |
2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.481+568C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141216 | |||||||
| chr3:3141310 | CAT | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0017g0051 others(1): Show |
4 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+663_481+664del others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141310 | |||||||
| chr3:3141337 | A | T | 1 | a0001c0001t0002g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.481+689A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141337 | |||||||
| chr3:3141451 | T | G | 1 | a0001c0002t0003g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.481+803T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141451 | |||||||
| chr3:3141453 | T | C | 7 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(4): Show |
8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.481+805T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141453 | |||||||
| chr3:3141542 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+894A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141542 | |||||||
| chr3:3141573 | T | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0075 others(3): Show |
24 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.481+925T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141573 | |||||||
| chr3:3141717 | C | G | 1 | a0004c0013t0026g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.481+1069C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141717 | |||||||
| chr3:3141736 | T | C | 1 | a0003c0014t0016g0151 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.481+1088T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141736 | |||||||
| chr3:3141887 | A | G | 1 | a0001c0001t0003g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.481+1239A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141887 | |||||||
| chr3:3141992 | G | A | 1 | a0001c0001t0025g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.481+1344G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141992 | |||||||
| chr3:3142100 | A | C | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.481+1452A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142100 | |||||||
| chr3:3142170 | T | C | 7 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(4): Show |
8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.481+1522T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142170 | |||||||
| chr3:3142258 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.481+1610T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142258 | |||||||
| chr3:3142382 | A | C | 1 | a0003c0014t0016g0151 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.481+1734A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142382 | |||||||
| chr3:3142476 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.481+1828C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142476 | |||||||
| chr3:3142623 | C | G | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.482-1961C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142623 | |||||||
| chr3:3142677 | C | T | 3 | a0001c0002t0003g0014 a0001c0002t0003g0143 a0001c0002t0003g0146 |
8 | HG00642.hp1 HG01168.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-1907C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142677 | |||||||
| chr3:3142758 | C | T | 18 | a0001c0001t0003g0163 a0001c0002t0003g0002 a0001c0002t0003g0011 others(15): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.482-1826C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142758 | |||||||
| chr3:3142894 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.482-1690C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142894 | |||||||
| chr3:3142969 | G | C | 72 | a0001c0001t0001g0122 a0001c0001t0002g0005 a0001c0001t0002g0007 others(69): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.482-1615G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142969 | |||||||
| chr3:3142971 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.482-1613A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142971 | |||||||
| chr3:3143028 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.482-1556G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143028 | |||||||
| chr3:3143229 | C | T | 19 | a0001c0001t0003g0163 a0001c0002t0003g0002 a0001c0002t0003g0011 others(16): Show |
54 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.482-1355C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143229 | |||||||
| chr3:3143241 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(138): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.482-1343A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143241 | |||||||
| chr3:3143301 | A | G | 19 | a0001c0001t0003g0163 a0001c0002t0003g0002 a0001c0002t0003g0011 others(16): Show |
54 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.482-1283A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143301 | |||||||
| chr3:3143308 | G | A | 1 | a0002c0003t0004g0043 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.482-1276G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143308 | |||||||
| chr3:3143353 | A | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0017g0051 others(2): Show |
5 | HG01106.hp2 HG01175.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1231A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143353 | |||||||
| chr3:3143509 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.482-1075A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143509 | |||||||
| chr3:3143520 | C | T | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.482-1064C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143520 | |||||||
| chr3:3143572 | C | T | 71 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(68): Show |
123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.482-1012C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143572 | |||||||
| chr3:3143592 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.482-992T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143592 | |||||||
| chr3:3143702 | AC | A | 75 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(72): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.482-879delC | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 3143702 | ||||||
| chr3:3143723 | C | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0077 others(4): Show |
14 | HG00673.hp1 HG03927.hp2 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-861C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143723 | |||||||
| chr3:3143829 | A | C | 73 | a0001c0001t0001g0059 a0001c0001t0002g0005 a0001c0001t0002g0007 others(70): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.482-755A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143829 | |||||||
| chr3:3143906 | A | G | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-678A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143906 | |||||||
| chr3:3144002 | T | A | 1 | a0001c0001t0018g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.482-582T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144002 | |||||||
| chr3:3144043 | A | T | 1 | a0001c0001t0002g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.482-541A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144043 | |||||||
| chr3:3144050 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.482-534T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144050 | |||||||
| chr3:3144292 | G | A | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.482-292G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144292 | |||||||
| chr3:3144381 | T | C | 1 | a0001c0001t0006g0129 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.482-203T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144381 | |||||||
| chr3:3144555 | ATT | A | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-25_482-24delTT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 3144555 | ||||||
| chr3:3144560 | T | A | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-24T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144560 | |||||||
| chr3:3144888 | T | C | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.608+178T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3144888 | |||||||
| chr3:3144895 | T | A | 1 | a0001c0001t0002g0110 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.608+185T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3144895 | |||||||
| chr3:3145035 | T | G | 17 | a0001c0002t0003g0002 a0001c0002t0003g0011 a0001c0002t0003g0014 others(14): Show |
52 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.608+325T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145035 | |||||||
| chr3:3145085 | T | C | 17 | a0001c0002t0003g0002 a0001c0002t0003g0011 a0001c0002t0003g0014 others(14): Show |
52 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.608+375T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145085 | |||||||
| chr3:3145088 | G | C | 72 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(69): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.608+378G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145088 | |||||||
| chr3:3145105 | G | C | 3 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0001c0001t0006g0048 |
4 | HG00280.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.608+395G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145105 | |||||||
| chr3:3145128 | G | A | 1 | a0004c0013t0026g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.608+418G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145128 | |||||||
| chr3:3145169 | C | G | 1 | a0001c0001t0017g0052 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.608+459C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145169 | |||||||
| chr3:3145210 | C | T | 18 | a0001c0001t0003g0163 a0001c0002t0003g0002 a0001c0002t0003g0011 others(15): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.608+500C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145210 | |||||||
| chr3:3145226 | C | T | 4 | a0001c0004t0008g0023 a0001c0004t0008g0044 a0001c0004t0008g0045 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.608+516C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145226 | |||||||
| chr3:3145255 | C | T | 1 | a0001c0002t0014g0039 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.608+545C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145255 | |||||||
| chr3:3145270 | C | T | 1 | a0001c0001t0012g0108 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.608+560C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145270 | |||||||
| chr3:3145271 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.608+561G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145271 | |||||||
| chr3:3145299 | T | TC | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.608+589_608+590ins others(1): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145299 | |||||||
| chr3:3145319 | T | C | 81 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0059 others(78): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.608+609T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145319 | |||||||
| chr3:3145322 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.608+612T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145322 | |||||||
| chr3:3145345 | T | C | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.608+635T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145345 | |||||||
| chr3:3145360 | A | G | 26 | a0001c0001t0001g0036 a0001c0001t0003g0163 a0001c0002t0003g0002 others(23): Show |
63 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.608+650A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145360 | |||||||
| chr3:3145375 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0007g0137 |
3 | HG01192.hp2 HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.608+665C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145375 | |||||||
| chr3:3145386 | C | T | 1 | a0001c0002t0003g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.608+676C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145386 | |||||||
| chr3:3145392 | A | C | 1 | a0001c0002t0003g0011 | 7 | HG00733.hp1 HG00735.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.608+682A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145392 | |||||||
| chr3:3145426 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0064 others(1): Show |
17 | HG00408.hp1 HG02080.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.608+716C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145426 | |||||||
| chr3:3145427 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.608+717C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145427 | |||||||
| chr3:3145465 | C | T | 1 | a0006c0011t0001g0085 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.608+755C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145465 | |||||||
| chr3:3145479 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.608+769G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145479 | |||||||
| chr3:3145481 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.608+771C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145481 | |||||||
| chr3:3145490 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.608+780G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145490 | |||||||
| chr3:3145502 | CA | C | 30 | a0001c0001t0001g0036 a0001c0001t0001g0061 a0001c0001t0001g0082 others(27): Show |
71 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.608+813delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 3145502 | ||||||
| chr3:3145502 | CAA | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(120): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.608+812_608+813del others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 3145502 | ||||||
| chr3:3145557 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.608+847G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145557 | |||||||
| chr3:3145732 | C | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.609-698C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145732 | |||||||
| chr3:3145893 | G | A | 1 | a0001c0002t0014g0039 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.609-537G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145893 | |||||||
| chr3:3145943 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.609-487C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145943 | |||||||
| chr3:3145959 | G | A | 18 | a0001c0001t0003g0163 a0001c0002t0003g0002 a0001c0002t0003g0011 others(15): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.609-471G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145959 | |||||||
| chr3:3145986 | TA | T | 18 | a0001c0001t0003g0163 a0001c0002t0003g0002 a0001c0002t0003g0011 others(15): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.609-442delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 3145986 | ||||||
| chr3:3145996 | A | G | 1 | a0001c0012t0003g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.609-434A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145996 | |||||||
| chr3:3146196 | T | C | 1 | a0001c0001t0002g0030 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.609-234T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3146196 | |||||||
| chr3:3146266 | G | A | 3 | a0001c0001t0002g0125 a0001c0001t0002g0128 a0001c0001t0002g0161 |
3 | NA18964.hp2 NA19012.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.609-164G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3146266 | |||||||
| chr3:3146295 | C | T | 1 | a0001c0001t0002g0037 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.609-135C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3146295 | |||||||
| chr3:3146332 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
179 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.609-98A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3146332 | |||||||
| chr3:3146678 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.802+55A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3146678 | |||||||
| chr3:3146919 | A | T | 2 | a0001c0002t0014g0039 a0005c0007t0014g0138 |
3 | HG02109.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.802+296A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3146919 | |||||||
| chr3:3147025 | C | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0129 a0001c0001t0006g0164 |
8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+402C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147025 | |||||||
| chr3:3147050 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.803-400T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147050 | |||||||
| chr3:3147065 | G | C | 2 | a0001c0004t0016g0152 a0003c0014t0016g0151 |
2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.803-385G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147065 | |||||||
| chr3:3147078 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.803-372C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147078 | |||||||
| chr3:3147217 | A | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.803-233A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147217 | |||||||
| chr3:3147230 | C | G | 72 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(69): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.803-220C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147230 | |||||||
| chr3:3147284 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.803-166A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147284 | |||||||
| chr3:3147375 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.803-75T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147375 | |||||||
| chr3:3147376 | G | A | 24 | a0001c0002t0003g0002 a0001c0002t0003g0011 a0001c0002t0003g0014 others(21): Show |
60 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.803-74G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147376 | |||||||
| chr3:3147392 | A | G | 1 | a0001c0002t0014g0039 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.803-58A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147392 | |||||||
| chr3:3147413 | C | A | 1 | a0001c0001t0025g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.803-37C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147413 | |||||||
| chr3:3147714 | A | G | 74 | a0001c0001t0001g0059 a0001c0001t0002g0005 a0001c0001t0002g0007 others(71): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1056+11A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147714 | |||||||
| chr3:3147734 | T | C | 1 | a0002c0003t0004g0157 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1056+31T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147734 | |||||||
| chr3:3147748 | G | A | 14 | a0001c0001t0002g0012 a0001c0001t0002g0022 a0001c0001t0002g0030 others(11): Show |
21 | HG00423.hp2 HG01106.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1056+45G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147748 | |||||||
| chr3:3147789 | G | T | 1 | a0002c0003t0004g0017 | 5 | HG02647.hp1 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056+86G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147789 | |||||||
| chr3:3147828 | G | A | 2 | a0001c0004t0008g0044 a0001c0004t0008g0045 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1057-78G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147828 |