Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9617 |
| ensemblid | ENSG00000120662.16 |
| hgncid | 7469 |
| symbol | MTRF1 |
| name | mitochondrial translation release factor 1 |
| refseq_nuc | NM_004294.4 |
| refseq_prot | NP_004285.2 |
| ensembl_nuc | ENST00000379480.9 |
| ensembl_prot | ENSP00000368793.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 41216369 |
| end | 41263576 |
| strand | - |
| ver | v1.2 |
| region | chr13:41216369-41263576 |
| region5000 | chr13:41211369-41268576 |
| regionname0 | MTRF1_chr13_41216369_41263576 |
| regionname5000 | MTRF1_chr13_41211369_41268576 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 445 | 309 | 71 | 46 | 157 | 9 | 24 | 125 | MTRF1_chr13_41211369_41268576 | MTRF1 | MNRHL others(440): Show |
chr13 | 41211369 | 41268576 |
| a0002 | 0/0 | 445 | 10 | 5 | 4 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | MSRHL others(440): Show |
chr13 | 41211369 | 41268576 |
| a0003 | 0/0 | 445 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | MSRHL others(440): Show |
chr13 | 41211369 | 41268576 |
| a0004 | 0/0 | 445 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | MSRHL others(440): Show |
chr13 | 41211369 | 41268576 |
| a0005 | 0/0 | 445 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | MNRHL others(440): Show |
chr13 | 41211369 | 41268576 |
| a0006 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | MSRHL others(440): Show |
chr13 | 41211369 | 41268576 |
| a0007 | 0/0 | 445 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | MNRHL others(440): Show |
chr13 | 41211369 | 41268576 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1335 | 175 | 45 | 29 | 85 | 5 | 10 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAA others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0001c0002 | 1/0 | 1335 | 130 | 23 | 16 | 72 | 4 | 14 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAA others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0001c0006 | 0/0 | 1335 | 3 | 3 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAA others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0001c0010 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAA others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0002c0003 | 0/0 | 1335 | 8 | 5 | 2 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAG others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0002c0008 | 0/0 | 1335 | 2 | 0 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAG others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0003c0004 | 0/0 | 1335 | 5 | 5 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAG others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0004c0005 | 0/0 | 1335 | 4 | 2 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAG others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0005c0007 | 0/0 | 1335 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAA others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0006c0011 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAG others(1330): Show |
chr13 | 41211369 | 41268576 | ||
| a0007c0009 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | ATGAA others(1330): Show |
chr13 | 41211369 | 41268576 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2184 | 152 | 37 | 29 | 70 | 5 | 10 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0001c0001t0002 | 0/0 | 2184 | 15 | 0 | 0 | 15 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0001c0001t0003 | 0/0 | 2184 | 6 | 6 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0001c0001t0005 | 0/0 | 2184 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0001c0001t0006 | 0/0 | 2184 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0001c0002t0001 | 1/0 | 2184 | 124 | 23 | 16 | 66 | 4 | 14 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0001c0002t0002 | 0/0 | 2184 | 6 | 0 | 0 | 6 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0001c0006t0003 | 0/0 | 2184 | 3 | 3 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0001c0010t0001 | 0/0 | 2184 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0002c0003t0001 | 0/0 | 2184 | 2 | 1 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0002c0003t0004 | 0/0 | 2184 | 6 | 4 | 1 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0002c0008t0001 | 0/0 | 2184 | 2 | 0 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0003c0004t0001 | 0/0 | 2184 | 5 | 5 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0004c0005t0001 | 0/0 | 2184 | 4 | 2 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0005c0007t0001 | 0/0 | 2184 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0006c0011t0003 | 0/0 | 2184 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| a0007c0009t0001 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | GTGAT others(2179): Show |
chr13 | 41211369 | 41268576 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0001 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0002 | 0/0 | 7 | 0 | 2 | 3 | 0 | 2 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0011 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0006t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0006t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0001c0010t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0003t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0003t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0003t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0003t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0003t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0008t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0002c0008t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0003c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0003c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0003c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0003c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0003c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0004c0005t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0004c0005t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0004c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0005c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0005c0007t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0006c0011t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| a0007c0009t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0011 | EUR | GBR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00280 | hp2 | a0002 | c0003 | t0004 | g0164 | EUR | FIN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01069 | hp1 | a0002 | c0008 | t0001 | g0266 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01071 | hp1 | a0002 | c0008 | t0001 | g0265 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01109 | hp1 | a0004 | c0005 | t0001 | g0175 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01169 | hp2 | a0001 | c0010 | t0001 | g0105 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01192 | hp1 | a0004 | c0005 | t0001 | g0176 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01192 | hp2 | a0002 | c0003 | t0004 | g0166 | AMR | PUR | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0028 | EUR | IBS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0217 | EUR | IBS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01891 | hp1 | a0003 | c0004 | t0001 | g0169 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0174 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02055 | hp1 | a0002 | c0003 | t0004 | g0165 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CDX | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | KHV | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02615 | hp1 | a0002 | c0003 | t0004 | g0168 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02622 | hp2 | a0005 | c0007 | t0001 | g0042 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0079 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02630 | hp2 | a0001 | c0006 | t0003 | g0037 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0199 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02717 | hp1 | a0005 | c0007 | t0001 | g0041 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02818 | hp1 | a0003 | c0004 | t0001 | g0172 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02818 | hp2 | a0006 | c0011 | t0003 | g0161 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0173 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02895 | hp2 | a0004 | c0005 | t0001 | g0026 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02897 | hp1 | a0004 | c0005 | t0001 | g0026 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02976 | hp1 | a0003 | c0004 | t0001 | g0171 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03453 | hp1 | a0003 | c0004 | t0001 | g0167 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03516 | hp1 | a0001 | c0006 | t0003 | g0016 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0264 | AFR | ESN | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | BEB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0220 | SAS | BEB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0241 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18522 | hp2 | a0003 | c0004 | t0001 | g0170 | AFR | YRI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | CHB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | YRI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18953 | hp2 | a0007 | c0009 | t0001 | g0064 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | TSI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | CLM | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02486 | hp1 | a0002 | c0003 | t0004 | g0162 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG02559 | hp2 | a0001 | c0006 | t0003 | g0016 | AFR | ACB | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | USA | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | USA | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA20300 | hp2 | a0002 | c0003 | t0004 | g0163 | AFR | USA | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0116 | REF | REF | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0232 | REF | REF | MTRF1_chr13_41211369_41268576 | MTRF1 | chr13 | 41211369 | 41268576 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:41217138 | C | T | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1315G>A | p.Glu439Lys | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 1415/2184 | 1315/1338 | 439/445 | chr13 | 41217138 | |||
| chr13:41217174 | A | C | 1 | a0003 | 5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.1279T>G | p.Ser427Ala | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 1379/2184 | 1279/1338 | 427/445 | chr13 | 41217174 | |||
| chr13:41223261 | T | C | 2 | a0004 a0005 |
6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
missense_variant | MODERATE | c.1219A>G | p.Ile407Val | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/10 | 1319/2184 | 1219/1338 | 407/445 | chr13 | 41223261 | |||
| chr13:41223350 | C | G | 1 | a0007 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.1130G>C | p.Gly377Ala | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/10 | 1230/2184 | 1130/1338 | 377/445 | chr13 | 41223350 | |||
| chr13:41260903 | T | C | 4 | a0002 a0003 a0004 others(1): Show |
20 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
missense_variant | MODERATE | c.5A>G | p.Asn2Ser | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/10 | 105/2184 | 5/1338 | 2/445 | chr13 | 41260903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:41240402 | G | A | 1 | a0001c0010 | 1 | HG01169.hp2 | synonymous_variant | LOW | c.729C>T | p.Ser243Ser | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/10 | 829/2184 | 729/1338 | 243/445 | chr13 | 41240402 | |||
| chr13:41252679 | T | C | 1 | a0001c0006 | 3 | HG02559.hp2 HG02630.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.663A>G | p.Gln221Gln | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/10 | 763/2184 | 663/1338 | 221/445 | chr13 | 41252679 | |||
| chr13:41252956 | A | T | 1 | a0002c0008 | 2 | HG01069.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.582T>A | p.Thr194Thr | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 4/10 | 682/2184 | 582/1338 | 194/445 | chr13 | 41252956 | |||
| chr13:41260608 | C | T | 10 | a0001c0001 a0001c0006 a0001c0010 others(7): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
synonymous_variant | LOW | c.300G>A | p.Glu100Glu | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/10 | 400/2184 | 300/1338 | 100/445 | chr13 | 41260608 | |||
| chr13:41260620 | G | A | 1 | a0004c0005 | 4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
synonymous_variant | LOW | c.288C>T | p.Ile96Ile | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/10 | 388/2184 | 288/1338 | 96/445 | chr13 | 41260620 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:41216448 | A | C | 1 | a0002c0003t0004 | 6 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*667T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 667 | chr13 | 41216448 | ||||||
| chr13:41216596 | C | A | 2 | a0001c0001t0002 a0001c0002t0002 |
21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*519G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 519 | chr13 | 41216596 | ||||||
| chr13:41216891 | T | G | 1 | a0001c0001t0006 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 224 | chr13 | 41216891 | ||||||
| chr13:41216980 | C | T | 1 | a0001c0001t0005 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*135G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 135 | chr13 | 41216980 | ||||||
| chr13:41217112 | T | C | 3 | a0001c0001t0003 a0001c0006t0003 a0006c0011t0003 |
10 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 10/10 | 3 | chr13 | 41217112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:41217304 | T | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(113): Show |
136 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1225-76A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217304 | |||||||
| chr13:41217434 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1225-206A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217434 | |||||||
| chr13:41217484 | A | G | 7 | a0001c0001t0003g0015 a0001c0001t0003g0033 a0001c0001t0003g0034 others(4): Show |
9 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-256T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217484 | |||||||
| chr13:41217619 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1225-391G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217619 | |||||||
| chr13:41217621 | TA | T | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-394delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41217621 | |||||||
| chr13:41218021 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1225-793A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218021 | |||||||
| chr13:41218121 | A | C | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1225-893T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218121 | |||||||
| chr13:41218280 | AATTTTTT others(11): Show |
A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | HG00280.hp1 HG00735.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-1070_1225-105 others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218280 | |||||||
| chr13:41218281 | A | AT | 30 | a0001c0001t0001g0018 a0001c0001t0003g0034 a0001c0002t0001g0001 others(27): Show |
35 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1225-1054dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | |||||||
| chr13:41218281 | AT | A | 8 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(5): Show |
8 | HG00280.hp2 HG02486.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.1225-1054delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | |||||||
| chr13:41218281 | ATT | A | 10 | a0001c0001t0001g0005 a0001c0001t0002g0003 a0001c0001t0002g0052 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1225-1055_1225-105 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | |||||||
| chr13:41218281 | ATTT | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0045 others(11): Show |
16 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1225-1056_1225-105 others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | |||||||
| chr13:41218281 | ATTTT | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0040 others(6): Show |
9 | HG01192.hp1 HG02165.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-1057_1225-105 others(8): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | |||||||
| chr13:41218281 | ATTTTTTT others(3): Show |
A | 2 | a0001c0002t0001g0007 a0001c0002t0001g0257 |
2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1225-1063_1225-105 others(14): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | |||||||
| chr13:41218281 | ATTTTTTT others(10): Show |
A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0060 others(5): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-1070_1225-105 others(21): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | |||||||
| chr13:41218281 | ATTTTTTT others(11): Show |
A | 103 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(100): Show |
122 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1225-1071_1225-105 others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218281 | |||||||
| chr13:41218299 | T | C | 5 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | HG00280.hp1 HG00735.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-1071A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218299 | |||||||
| chr13:41218355 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1225-1127G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218355 | |||||||
| chr13:41218486 | A | T | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1225-1258T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218486 | |||||||
| chr13:41218504 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1225-1276T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218504 | |||||||
| chr13:41218782 | T | C | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1225-1554A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218782 | |||||||
| chr13:41218842 | T | TTTTGAGA others(17): Show |
1 | a0001c0002t0001g0183 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1225-1615_1225-161 others(28): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218842 | |||||||
| chr13:41218870 | T | C | 1 | a0001c0002t0001g0183 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1225-1642A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41218870 | |||||||
| chr13:41219062 | G | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(3): Show |
6 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1225-1834C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219062 | |||||||
| chr13:41219114 | AACCCCGT others(25): Show |
A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
178 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.1225-1918_1225-188 others(36): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219114 | |||||||
| chr13:41219119 | C | T | 2 | a0001c0001t0005g0160 a0001c0002t0001g0205 |
2 | HG03041.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1225-1891G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219119 | |||||||
| chr13:41219120 | G | A | 1 | a0002c0003t0001g0174 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1225-1892C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219120 | |||||||
| chr13:41219149 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-1921C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219149 | |||||||
| chr13:41219290 | CAA | C | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1225-2064_1225-206 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219290 | |||||||
| chr13:41219308 | T | C | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1225-2080A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219308 | |||||||
| chr13:41219374 | T | C | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-2146A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219374 | |||||||
| chr13:41219598 | G | C | 6 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0211 others(3): Show |
6 | NA18977.hp2 NA19003.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1225-2370C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219598 | |||||||
| chr13:41219619 | A | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(108): Show |
130 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1225-2391T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219619 | |||||||
| chr13:41219673 | A | T | 1 | a0001c0002t0001g0263 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1225-2445T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219673 | |||||||
| chr13:41219674 | T | A | 1 | a0001c0002t0001g0263 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1225-2446A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219674 | |||||||
| chr13:41219695 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1225-2467G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219695 | |||||||
| chr13:41219696 | A | G | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
178 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.1225-2468T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219696 | |||||||
| chr13:41219789 | G | A | 1 | a0002c0003t0001g0174 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1225-2561C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219789 | |||||||
| chr13:41219863 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1225-2635A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219863 | |||||||
| chr13:41219912 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-2684G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219912 | |||||||
| chr13:41219998 | C | CA | 26 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0046 others(23): Show |
34 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1225-2771dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219998 | |||||||
| chr13:41219998 | C | CAA | 75 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
88 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1225-2772_1225-277 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219998 | |||||||
| chr13:41219998 | C | CAAA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(32): Show |
42 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1225-2773_1225-277 others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219998 | |||||||
| chr13:41219998 | CA | C | 98 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0048 others(95): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1225-2771delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41219998 | |||||||
| chr13:41220125 | C | T | 26 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(23): Show |
32 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1225-2897G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220125 | |||||||
| chr13:41220236 | A | G | 1 | a0001c0001t0003g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1225-3008T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220236 | |||||||
| chr13:41220252 | C | A | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1224+3004G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220252 | |||||||
| chr13:41220322 | CG | C | 53 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0038 others(50): Show |
63 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1224+2933delC | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220322 | |||||||
| chr13:41220323 | G | GA | 9 | a0001c0001t0003g0015 a0001c0001t0003g0034 a0001c0006t0003g0016 others(6): Show |
9 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1224+2932_1224+293 others(5): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220323 | |||||||
| chr13:41220323 | G | GAA | 3 | a0002c0003t0001g0173 a0002c0003t0001g0174 a0002c0003t0004g0165 |
3 | HG01981.hp1 HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1224+2932_1224+293 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220323 | |||||||
| chr13:41220323 | GGA | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(92): Show |
115 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1224+2931_1224+293 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220323 | |||||||
| chr13:41220324 | G | A | 23 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0002g0053 others(20): Show |
25 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1224+2932C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220324 | |||||||
| chr13:41220324 | G | GA | 23 | a0001c0002t0001g0181 a0001c0002t0001g0187 a0001c0002t0001g0190 others(20): Show |
23 | HG00423.hp1 HG00735.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1224+2931dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220324 | |||||||
| chr13:41220395 | G | A | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+2861C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220395 | |||||||
| chr13:41220413 | G | A | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224+2843C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220413 | |||||||
| chr13:41220615 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1224+2641G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220615 | |||||||
| chr13:41220734 | C | G | 1 | a0001c0001t0003g0033 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1224+2522G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41220734 | |||||||
| chr13:41221087 | T | C | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224+2169A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221087 | |||||||
| chr13:41221156 | C | CT | 8 | a0001c0001t0002g0053 a0001c0002t0001g0028 a0001c0002t0001g0208 others(5): Show |
9 | HG01261.hp2 HG01515.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1224+2099dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221156 | |||||||
| chr13:41221323 | A | AT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1224+1932dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221323 | |||||||
| chr13:41221425 | G | T | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1224+1831C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221425 | |||||||
| chr13:41221448 | G | A | 5 | a0001c0002t0001g0028 a0001c0002t0001g0208 a0001c0002t0001g0217 others(2): Show |
6 | HG01261.hp2 HG01515.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1224+1808C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221448 | |||||||
| chr13:41221599 | T | C | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1224+1657A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221599 | |||||||
| chr13:41221812 | C | T | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1224+1444G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221812 | |||||||
| chr13:41221830 | T | TACC | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1224+1425_1224+142 others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221830 | |||||||
| chr13:41221886 | C | T | 1 | a0001c0002t0001g0216 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1224+1370G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41221886 | |||||||
| chr13:41222104 | T | C | 54 | a0001c0001t0001g0025 a0001c0001t0001g0143 a0001c0001t0001g0144 others(51): Show |
67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1224+1152A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222104 | |||||||
| chr13:41222406 | G | A | 13 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(10): Show |
13 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1224+850C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222406 | |||||||
| chr13:41222433 | A | G | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+823T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222433 | |||||||
| chr13:41222486 | A | C | 8 | a0001c0001t0003g0015 a0001c0001t0003g0033 a0001c0001t0003g0034 others(5): Show |
10 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224+770T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222486 | |||||||
| chr13:41222543 | C | T | 1 | a0001c0001t0006g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1224+713G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222543 | |||||||
| chr13:41222676 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(3): Show |
10 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1224+580G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222676 | |||||||
| chr13:41222940 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1224+316G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41222940 | |||||||
| chr13:41223055 | T | C | 1 | a0001c0001t0003g0034 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1224+201A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 9/9 | chr13 | 41223055 | |||||||
| chr13:41223465 | A | T | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1126-111T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223465 | |||||||
| chr13:41223519 | T | C | 1 | a0001c0002t0001g0260 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1126-165A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223519 | |||||||
| chr13:41223536 | C | T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(13): Show |
21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.1126-182G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223536 | |||||||
| chr13:41223609 | T | C | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1126-255A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223609 | |||||||
| chr13:41223794 | C | T | 5 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 others(2): Show |
6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-440G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223794 | |||||||
| chr13:41223798 | T | C | 5 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 others(2): Show |
6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-444A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223798 | |||||||
| chr13:41223847 | C | T | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1126-493G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41223847 | |||||||
| chr13:41224344 | C | G | 1 | a0001c0002t0001g0216 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1126-990G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224344 | |||||||
| chr13:41224408 | A | G | 5 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-1054T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224408 | |||||||
| chr13:41224421 | T | C | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1126-1067A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224421 | |||||||
| chr13:41224439 | G | A | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1126-1085C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224439 | |||||||
| chr13:41224562 | C | A | 1 | a0003c0004t0001g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1126-1208G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224562 | |||||||
| chr13:41224685 | G | A | 2 | a0001c0002t0001g0028 a0001c0002t0001g0259 |
3 | HG01515.hp1 HG02004.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1126-1331C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224685 | |||||||
| chr13:41224735 | G | A | 5 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-1381C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224735 | |||||||
| chr13:41224784 | C | T | 5 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-1430G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224784 | |||||||
| chr13:41224842 | T | C | 5 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 others(2): Show |
6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-1488A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41224842 | |||||||
| chr13:41225009 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(113): Show |
136 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1125+1423G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225009 | |||||||
| chr13:41225038 | CCCAT | C | 4 | a0001c0002t0001g0179 a0001c0002t0001g0189 a0001c0002t0001g0190 others(1): Show |
4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+1390_1125+139 others(8): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225038 | |||||||
| chr13:41225105 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1125+1327C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225105 | |||||||
| chr13:41225107 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(113): Show |
136 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1125+1325C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225107 | |||||||
| chr13:41225209 | C | CA | 144 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(141): Show |
170 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1125+1222dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225209 | |||||||
| chr13:41225209 | C | CAA | 27 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0019 others(24): Show |
33 | HG00280.hp2 HG01109.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1125+1221_1125+122 others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225209 | |||||||
| chr13:41225229 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1125+1203G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225229 | |||||||
| chr13:41225235 | G | A | 2 | a0001c0002t0001g0224 a0001c0002t0001g0260 |
2 | HG00558.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1125+1197C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225235 | |||||||
| chr13:41225322 | G | A | 26 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(23): Show |
32 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1125+1110C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225322 | |||||||
| chr13:41225363 | G | A | 4 | a0001c0002t0001g0179 a0001c0002t0001g0189 a0001c0002t0001g0190 others(1): Show |
4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+1069C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225363 | |||||||
| chr13:41225520 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1125+912C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225520 | |||||||
| chr13:41225808 | T | TA | 9 | a0001c0001t0005g0160 a0001c0002t0001g0191 a0001c0002t0001g0245 others(6): Show |
9 | HG00280.hp2 HG01192.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1125+623dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225808 | |||||||
| chr13:41225808 | TA | T | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
153 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1125+623delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225808 | |||||||
| chr13:41225808 | TAA | T | 24 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(21): Show |
29 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1125+622_1125+623d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225808 | |||||||
| chr13:41225951 | G | T | 1 | a0001c0001t0001g0147 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1125+481C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225951 | |||||||
| chr13:41225959 | T | TG | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1125+472dupC | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225959 | |||||||
| chr13:41225970 | GAAAAAT | G | 5 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 others(2): Show |
6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+456_1125+461d others(8): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41225970 | |||||||
| chr13:41226151 | G | A | 5 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 others(2): Show |
6 | HG01109.hp1 HG01192.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+281C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41226151 | |||||||
| chr13:41226262 | T | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(108): Show |
130 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1125+170A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41226262 | |||||||
| chr13:41226292 | A | G | 8 | a0001c0002t0001g0013 a0001c0002t0001g0029 a0001c0002t0001g0230 others(5): Show |
11 | HG01952.hp2 HG01993.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1125+140T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 8/9 | chr13 | 41226292 | |||||||
| chr13:41226857 | T | C | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.989-289A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41226857 | |||||||
| chr13:41226912 | G | A | 15 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(12): Show |
20 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(17): Show |
intron_variant | MODIFIER | c.989-344C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41226912 | |||||||
| chr13:41227003 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.989-435A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227003 | |||||||
| chr13:41227084 | A | T | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.989-516T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227084 | |||||||
| chr13:41227158 | G | A | 8 | a0001c0001t0003g0015 a0001c0001t0003g0033 a0001c0001t0003g0034 others(5): Show |
10 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.989-590C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227158 | |||||||
| chr13:41227413 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.989-845C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227413 | |||||||
| chr13:41227467 | T | A | 146 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
176 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.989-899A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227467 | |||||||
| chr13:41227484 | A | G | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
177 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.989-916T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227484 | |||||||
| chr13:41227588 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.989-1020A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227588 | |||||||
| chr13:41227903 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.989-1335G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41227903 | |||||||
| chr13:41228000 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.989-1432G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228000 | |||||||
| chr13:41228002 | A | G | 1 | a0001c0002t0001g0204 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.989-1434T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228002 | |||||||
| chr13:41228009 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.989-1441C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228009 | |||||||
| chr13:41228171 | CT | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(112): Show |
135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.989-1604delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228171 | |||||||
| chr13:41228259 | G | C | 5 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0103 others(2): Show |
5 | NA18963.hp1 NA18987.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-1691C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228259 | |||||||
| chr13:41228308 | G | A | 2 | a0001c0002t0001g0203 a0001c0002t0001g0206 |
2 | NA18969.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.989-1740C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228308 | |||||||
| chr13:41228374 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.989-1806G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228374 | |||||||
| chr13:41228415 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0075 others(1): Show |
5 | HG02615.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-1847T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228415 | |||||||
| chr13:41228428 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.989-1860C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228428 | |||||||
| chr13:41228637 | TAA | T | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
177 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.989-2071_989-2070d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228637 | |||||||
| chr13:41228710 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01070.hp1 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.989-2142T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228710 | |||||||
| chr13:41228772 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.989-2204C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228772 | |||||||
| chr13:41228809 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.989-2241T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228809 | |||||||
| chr13:41228895 | T | C | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.989-2327A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41228895 | |||||||
| chr13:41229021 | A | G | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.989-2453T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229021 | |||||||
| chr13:41229030 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.989-2462A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229030 | |||||||
| chr13:41229101 | C | A | 4 | a0001c0002t0001g0185 a0001c0002t0001g0186 a0001c0002t0001g0187 others(1): Show |
4 | HG02055.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-2533G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229101 | |||||||
| chr13:41229147 | G | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.989-2579C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229147 | |||||||
| chr13:41229235 | G | A | 1 | a0001c0002t0001g0215 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.989-2667C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229235 | |||||||
| chr13:41229253 | C | T | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.989-2685G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229253 | |||||||
| chr13:41229543 | ACT | A | 5 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.989-2977_989-2976d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229543 | |||||||
| chr13:41229569 | G | A | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.989-3001C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229569 | |||||||
| chr13:41229685 | T | A | 23 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(20): Show |
28 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.989-3117A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229685 | |||||||
| chr13:41229822 | C | T | 1 | a0006c0011t0003g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.989-3254G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229822 | |||||||
| chr13:41229850 | C | T | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.989-3282G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229850 | |||||||
| chr13:41229898 | C | T | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.989-3330G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229898 | |||||||
| chr13:41229918 | T | C | 1 | a0001c0002t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.989-3350A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229918 | |||||||
| chr13:41229950 | A | G | 1 | a0002c0003t0004g0164 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.989-3382T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41229950 | |||||||
| chr13:41230013 | A | C | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-3445T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230013 | |||||||
| chr13:41230105 | G | GA | 28 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(25): Show |
35 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.989-3538dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230105 | |||||||
| chr13:41230115 | A | C | 1 | a0001c0002t0001g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.989-3547T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230115 | |||||||
| chr13:41230182 | A | T | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-3614T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230182 | |||||||
| chr13:41230183 | T | G | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-3615A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230183 | |||||||
| chr13:41230325 | C | T | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.988+3565G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230325 | |||||||
| chr13:41230350 | T | G | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+3540A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230350 | |||||||
| chr13:41230563 | C | CT | 14 | a0001c0001t0001g0031 a0001c0001t0001g0069 a0001c0001t0003g0015 others(11): Show |
16 | HG01261.hp1 HG02004.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.988+3326dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230563 | |||||||
| chr13:41230625 | A | C | 1 | a0002c0003t0004g0164 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.988+3265T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230625 | |||||||
| chr13:41230684 | A | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
187 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.988+3206T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230684 | |||||||
| chr13:41230716 | G | A | 4 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0225 others(1): Show |
4 | HG00558.hp2 NA18953.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+3174C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230716 | |||||||
| chr13:41230726 | C | CT | 109 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(106): Show |
128 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.988+3163dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230726 | |||||||
| chr13:41230953 | G | C | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.988+2937C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41230953 | |||||||
| chr13:41231016 | G | A | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.988+2874C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231016 | |||||||
| chr13:41231029 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.988+2861T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231029 | |||||||
| chr13:41231120 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0048 |
3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.988+2770G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231120 | |||||||
| chr13:41231206 | T | G | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.988+2684A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231206 | |||||||
| chr13:41231370 | G | A | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.988+2520C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231370 | |||||||
| chr13:41231435 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.988+2455A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231435 | |||||||
| chr13:41231498 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0048 |
3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.988+2392C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231498 | |||||||
| chr13:41231618 | C | G | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
179 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.988+2272G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231618 | |||||||
| chr13:41231739 | C | G | 1 | a0001c0002t0001g0178 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.988+2151G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231739 | |||||||
| chr13:41231878 | C | CA | 11 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(8): Show |
15 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.988+2011dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231878 | |||||||
| chr13:41231878 | CA | C | 140 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(137): Show |
164 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.988+2011delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231878 | |||||||
| chr13:41231878 | CAA | C | 6 | a0001c0001t0001g0095 a0003c0004t0001g0167 a0003c0004t0001g0169 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+2010_988+2011d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231878 | |||||||
| chr13:41231897 | A | G | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.988+1993T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231897 | |||||||
| chr13:41231944 | C | A | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.988+1946G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231944 | |||||||
| chr13:41231989 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
5 | HG02451.hp2 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.988+1901G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41231989 | |||||||
| chr13:41232042 | C | T | 23 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(20): Show |
28 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.988+1848G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232042 | |||||||
| chr13:41232164 | G | A | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.988+1726C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232164 | |||||||
| chr13:41232192 | TA | T | 2 | a0001c0002t0001g0011 a0001c0002t0001g0220 |
4 | HG00140.hp2 HG03831.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+1697delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232192 | |||||||
| chr13:41232324 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.988+1566G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232324 | |||||||
| chr13:41232332 | CAA | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(134): Show |
162 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.988+1556_988+1557d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232332 | |||||||
| chr13:41232369 | G | A | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.988+1521C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232369 | |||||||
| chr13:41232374 | C | T | 4 | a0001c0002t0001g0185 a0001c0002t0001g0186 a0001c0002t0001g0187 others(1): Show |
4 | HG02055.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+1516G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232374 | |||||||
| chr13:41232398 | C | T | 1 | a0001c0002t0001g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.988+1492G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232398 | |||||||
| chr13:41232547 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.988+1343G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232547 | |||||||
| chr13:41232764 | C | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0048 |
3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.988+1126G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41232764 | |||||||
| chr13:41233462 | C | T | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.988+428G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233462 | |||||||
| chr13:41233463 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.988+427C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233463 | |||||||
| chr13:41233654 | C | G | 1 | a0001c0002t0001g0197 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.988+236G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233654 | |||||||
| chr13:41233676 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.988+214G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233676 | |||||||
| chr13:41233754 | C | T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(13): Show |
21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.988+136G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233754 | |||||||
| chr13:41233814 | T | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.988+76A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 7/9 | chr13 | 41233814 | |||||||
| chr13:41234204 | G | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-197C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41234204 | |||||||
| chr13:41234377 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.871-370G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41234377 | |||||||
| chr13:41234392 | T | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.871-385A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41234392 | |||||||
| chr13:41234508 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.871-501C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41234508 | |||||||
| chr13:41235092 | A | AT | 9 | a0001c0001t0005g0160 a0001c0002t0001g0181 a0001c0002t0001g0193 others(6): Show |
10 | HG01109.hp1 HG01192.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.871-1086dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235092 | |||||||
| chr13:41235092 | AT | A | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.871-1086delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235092 | |||||||
| chr13:41235235 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.871-1228A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235235 | |||||||
| chr13:41235335 | C | A | 9 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0003g0015 others(6): Show |
11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.871-1328G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235335 | |||||||
| chr13:41235814 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0075 others(1): Show |
5 | HG02615.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-1807G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235814 | |||||||
| chr13:41235840 | G | GAC | 39 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0038 others(36): Show |
51 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.871-1835_871-1834d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235840 | |||||||
| chr13:41235840 | G | GACACACA others(13): Show |
1 | a0001c0001t0001g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.871-1834_871-1833i others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235840 | |||||||
| chr13:41235854 | C | CAT | 110 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
129 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.871-1848_871-1847i others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235854 | |||||||
| chr13:41235854 | C | CATAG | 4 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0075 others(1): Show |
5 | HG02615.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-1848_871-1847i others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235854 | |||||||
| chr13:41235856 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0075 others(1): Show |
5 | HG02615.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-1849C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235856 | |||||||
| chr13:41235956 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.871-1949A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41235956 | |||||||
| chr13:41236001 | G | A | 23 | a0001c0002t0001g0012 a0001c0002t0001g0027 a0001c0002t0001g0183 others(20): Show |
26 | HG00558.hp2 HG01123.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.871-1994C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236001 | |||||||
| chr13:41236046 | C | G | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.871-2039G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236046 | |||||||
| chr13:41236081 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.871-2074T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236081 | |||||||
| chr13:41236120 | G | GT | 108 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(105): Show |
127 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.871-2114dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236120 | |||||||
| chr13:41236121 | T | G | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.871-2114A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236121 | |||||||
| chr13:41236412 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0150 |
4 | HG01884.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2405G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236412 | |||||||
| chr13:41236495 | G | A | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.871-2488C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236495 | |||||||
| chr13:41236598 | T | G | 3 | a0001c0002t0001g0028 a0001c0002t0001g0259 a0001c0002t0001g0263 |
4 | HG01515.hp1 HG02004.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2591A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236598 | |||||||
| chr13:41236666 | A | G | 1 | a0001c0002t0001g0226 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.871-2659T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236666 | |||||||
| chr13:41236940 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.871-2933G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236940 | |||||||
| chr13:41236944 | A | G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.871-2937T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236944 | |||||||
| chr13:41236975 | C | T | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-2968G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41236975 | |||||||
| chr13:41237166 | C | A | 2 | a0001c0002t0001g0200 a0001c0002t0001g0267 |
2 | NA18962.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.870+3095G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237166 | |||||||
| chr13:41237218 | C | CA | 28 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0019 others(25): Show |
34 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.870+3042dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237218 | |||||||
| chr13:41237218 | C | CAA | 103 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(100): Show |
123 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.870+3041_870+3042d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237218 | |||||||
| chr13:41237218 | C | CAAA | 9 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0082 others(6): Show |
9 | HG02145.hp2 HG02622.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.870+3040_870+3042d others(5): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237218 | |||||||
| chr13:41237218 | CA | C | 18 | a0001c0001t0002g0003 a0001c0001t0002g0051 a0001c0001t0002g0053 others(15): Show |
23 | HG02165.hp2 HG03453.hp1 NA18941.hp1 others(20): Show |
intron_variant | MODIFIER | c.870+3042delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237218 | |||||||
| chr13:41237306 | C | G | 5 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+2955G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237306 | |||||||
| chr13:41237436 | AATAAC | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+2820_870+2824d others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237436 | |||||||
| chr13:41237462 | C | T | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.870+2799G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237462 | |||||||
| chr13:41237643 | C | T | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.870+2618G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237643 | |||||||
| chr13:41237646 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.870+2615C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237646 | |||||||
| chr13:41237670 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.870+2591G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237670 | |||||||
| chr13:41237671 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0137 others(5): Show |
11 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.870+2590C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237671 | |||||||
| chr13:41237740 | C | T | 1 | a0001c0002t0001g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.870+2521G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237740 | |||||||
| chr13:41237879 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+2382C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237879 | |||||||
| chr13:41237899 | A | G | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2362T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237899 | |||||||
| chr13:41237917 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.870+2344T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41237917 | |||||||
| chr13:41238081 | T | C | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+2180A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238081 | |||||||
| chr13:41238229 | G | T | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.870+2032C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238229 | |||||||
| chr13:41238280 | T | A | 1 | a0001c0002t0001g0230 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.870+1981A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238280 | |||||||
| chr13:41238301 | G | A | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.870+1960C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238301 | |||||||
| chr13:41238493 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+1768T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238493 | |||||||
| chr13:41238635 | G | A | 23 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(20): Show |
28 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.870+1626C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238635 | |||||||
| chr13:41238696 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.870+1565C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238696 | |||||||
| chr13:41238890 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0048 |
3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.870+1371T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238890 | |||||||
| chr13:41238909 | G | A | 1 | a0001c0002t0001g0030 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.870+1352C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238909 | |||||||
| chr13:41238964 | G | A | 1 | a0006c0011t0003g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.870+1297C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41238964 | |||||||
| chr13:41239017 | T | TA | 9 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0003g0015 others(6): Show |
11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.870+1243dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239017 | |||||||
| chr13:41239091 | G | A | 2 | a0001c0002t0001g0223 a0001c0002t0001g0225 |
2 | NA18979.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.870+1170C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239091 | |||||||
| chr13:41239353 | T | A | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.870+908A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239353 | |||||||
| chr13:41239359 | C | T | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.870+902G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239359 | |||||||
| chr13:41239363 | G | A | 15 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0002c0003t0004g0162 others(12): Show |
16 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.870+898C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239363 | |||||||
| chr13:41239622 | G | C | 15 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0002c0003t0004g0162 others(12): Show |
16 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.870+639C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239622 | |||||||
| chr13:41239708 | T | G | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.870+553A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239708 | |||||||
| chr13:41239859 | C | G | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.870+402G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239859 | |||||||
| chr13:41239900 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+361G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239900 | |||||||
| chr13:41239958 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.870+303G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239958 | |||||||
| chr13:41239978 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.870+283A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41239978 | |||||||
| chr13:41240032 | G | A | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.870+229C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240032 | |||||||
| chr13:41240117 | C | T | 1 | a0001c0002t0001g0239 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.870+144G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240117 | |||||||
| chr13:41240141 | C | T | 145 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
175 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.870+120G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240141 | |||||||
| chr13:41240162 | C | CA | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.870+98dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240162 | |||||||
| chr13:41240219 | G | A | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+42C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 6/9 | chr13 | 41240219 | |||||||
| chr13:41240525 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0043 |
4 | HG02572.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.698-92C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240525 | |||||||
| chr13:41240573 | TGAA | T | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-143_698-141del others(3): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240573 | |||||||
| chr13:41240668 | T | A | 8 | a0001c0001t0001g0031 a0001c0001t0003g0015 a0001c0001t0003g0033 others(5): Show |
10 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.698-235A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240668 | |||||||
| chr13:41240697 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0048 |
3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.698-264T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240697 | |||||||
| chr13:41240934 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.698-501T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41240934 | |||||||
| chr13:41241157 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.698-724C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241157 | |||||||
| chr13:41241206 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.698-773C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241206 | |||||||
| chr13:41241248 | G | A | 6 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(3): Show |
6 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.698-815C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241248 | |||||||
| chr13:41241580 | T | C | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.698-1147A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241580 | |||||||
| chr13:41241700 | G | C | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-1267C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241700 | |||||||
| chr13:41241772 | G | C | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.698-1339C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241772 | |||||||
| chr13:41241909 | A | G | 4 | a0001c0001t0003g0033 a0001c0001t0003g0035 a0001c0006t0003g0016 others(1): Show |
5 | HG02559.hp2 HG02630.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-1476T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41241909 | |||||||
| chr13:41242105 | T | C | 261 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.698-1672A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242105 | |||||||
| chr13:41242123 | C | T | 1 | a0006c0011t0003g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.698-1690G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242123 | |||||||
| chr13:41242126 | CG | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.698-1694delC | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242126 | |||||||
| chr13:41242127 | G | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.698-1694C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242127 | |||||||
| chr13:41242127 | G | GT | 7 | a0001c0002t0001g0014 a0001c0002t0001g0180 a0001c0002t0001g0183 others(4): Show |
7 | HG01123.hp2 HG01496.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.698-1695dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242127 | |||||||
| chr13:41242127 | G | T | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.698-1694C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242127 | |||||||
| chr13:41242128 | T | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.698-1695A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242128 | |||||||
| chr13:41242151 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.698-1718G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242151 | |||||||
| chr13:41242234 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.698-1801G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242234 | |||||||
| chr13:41242245 | A | G | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1812T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242245 | |||||||
| chr13:41242554 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0048 |
3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.698-2121G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242554 | |||||||
| chr13:41242667 | G | A | 16 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(13): Show |
21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.698-2234C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242667 | |||||||
| chr13:41242751 | T | C | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-2318A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242751 | |||||||
| chr13:41242763 | G | A | 1 | a0002c0003t0004g0166 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.698-2330C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242763 | |||||||
| chr13:41242784 | C | T | 1 | a0001c0002t0001g0192 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.698-2351G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242784 | |||||||
| chr13:41242787 | C | T | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-2354G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242787 | |||||||
| chr13:41242849 | T | C | 159 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(156): Show |
191 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.698-2416A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242849 | |||||||
| chr13:41242852 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0117 |
2 | HG01934.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.698-2419C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242852 | |||||||
| chr13:41242941 | T | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.698-2508A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41242941 | |||||||
| chr13:41243017 | G | A | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.698-2584C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243017 | |||||||
| chr13:41243103 | C | T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(13): Show |
21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.698-2670G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243103 | |||||||
| chr13:41243108 | A | C | 1 | a0001c0002t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.698-2675T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243108 | |||||||
| chr13:41243129 | G | T | 1 | a0001c0001t0001g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.698-2696C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243129 | |||||||
| chr13:41243168 | A | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
185 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.698-2735T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243168 | |||||||
| chr13:41243238 | A | T | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
188 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.698-2805T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243238 | |||||||
| chr13:41243404 | C | CA | 112 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(109): Show |
133 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.698-2972dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243404 | |||||||
| chr13:41243404 | C | CAA | 8 | a0001c0001t0001g0073 a0001c0001t0001g0119 a0001c0001t0001g0122 others(5): Show |
8 | HG00438.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.698-2973_698-2972d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243404 | |||||||
| chr13:41243404 | CA | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(29): Show |
42 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.698-2972delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243404 | |||||||
| chr13:41243484 | G | A | 8 | a0001c0001t0001g0031 a0001c0001t0003g0015 a0001c0001t0003g0033 others(5): Show |
10 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.698-3051C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243484 | |||||||
| chr13:41243513 | C | G | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-3080G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243513 | |||||||
| chr13:41243515 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.698-3082C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243515 | |||||||
| chr13:41243523 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.698-3090G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243523 | |||||||
| chr13:41243973 | C | T | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.698-3540G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243973 | |||||||
| chr13:41243977 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0048 |
3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.698-3544A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41243977 | |||||||
| chr13:41244123 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.698-3690G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244123 | |||||||
| chr13:41244140 | T | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.698-3707A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244140 | |||||||
| chr13:41244166 | T | C | 1 | a0001c0002t0001g0196 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.698-3733A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244166 | |||||||
| chr13:41244220 | ACTTT | A | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.698-3791_698-3788d others(6): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244220 | |||||||
| chr13:41244238 | A | T | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-3805T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244238 | |||||||
| chr13:41244292 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.698-3859G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244292 | |||||||
| chr13:41244326 | C | T | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-3893G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244326 | |||||||
| chr13:41244407 | G | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.698-3974C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244407 | |||||||
| chr13:41244460 | T | G | 3 | a0001c0001t0005g0160 a0002c0003t0001g0173 a0002c0003t0001g0174 |
3 | HG01981.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.698-4027A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244460 | |||||||
| chr13:41244464 | C | T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(13): Show |
21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.698-4031G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244464 | |||||||
| chr13:41244608 | A | C | 4 | a0001c0002t0001g0179 a0001c0002t0001g0189 a0001c0002t0001g0190 others(1): Show |
4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-4175T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244608 | |||||||
| chr13:41244665 | C | T | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-4232G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244665 | |||||||
| chr13:41244738 | T | G | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-4305A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244738 | |||||||
| chr13:41244748 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.698-4315T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244748 | |||||||
| chr13:41244756 | G | C | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-4323C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244756 | |||||||
| chr13:41244807 | C | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG00544.hp2 NA18953.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.698-4374G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244807 | |||||||
| chr13:41244833 | A | G | 16 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(13): Show |
21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.698-4400T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244833 | |||||||
| chr13:41244841 | C | T | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.698-4408G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41244841 | |||||||
| chr13:41245004 | C | G | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-4571G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245004 | |||||||
| chr13:41245228 | A | G | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.698-4795T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245228 | |||||||
| chr13:41245249 | C | CT | 117 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(114): Show |
138 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.698-4817dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245249 | |||||||
| chr13:41245259 | T | C | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.698-4826A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245259 | |||||||
| chr13:41245405 | T | C | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.698-4972A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245405 | |||||||
| chr13:41245618 | T | C | 1 | a0001c0002t0001g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.698-5185A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245618 | |||||||
| chr13:41245751 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.698-5318A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41245751 | |||||||
| chr13:41246044 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0158 |
3 | NA18945.hp1 NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.698-5611C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246044 | |||||||
| chr13:41246049 | CT | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.698-5617delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246049 | |||||||
| chr13:41246069 | C | T | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.698-5636G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246069 | |||||||
| chr13:41246102 | T | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0120 a0001c0001t0001g0121 |
4 | HG01934.hp1 HG02083.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-5669A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246102 | |||||||
| chr13:41246241 | T | C | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.698-5808A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246241 | |||||||
| chr13:41246255 | G | C | 1 | a0001c0001t0001g0125 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.698-5822C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246255 | |||||||
| chr13:41246578 | T | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.697+6067A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246578 | |||||||
| chr13:41246590 | T | G | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.697+6055A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246590 | |||||||
| chr13:41246675 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0122 |
2 | HG00558.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.697+5970A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246675 | |||||||
| chr13:41246766 | C | T | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.697+5879G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246766 | |||||||
| chr13:41246824 | A | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.697+5821T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246824 | |||||||
| chr13:41246834 | G | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.697+5811C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246834 | |||||||
| chr13:41246867 | C | T | 4 | a0001c0001t0005g0160 a0002c0003t0001g0173 a0002c0003t0001g0174 others(1): Show |
4 | HG01981.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+5778G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246867 | |||||||
| chr13:41246939 | C | T | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.697+5706G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41246939 | |||||||
| chr13:41247032 | T | C | 1 | a0001c0002t0001g0231 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.697+5613A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247032 | |||||||
| chr13:41247041 | T | A | 1 | a0001c0002t0001g0183 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.697+5604A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247041 | |||||||
| chr13:41247143 | C | T | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.697+5502G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247143 | |||||||
| chr13:41247144 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0048 |
3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.697+5501C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247144 | |||||||
| chr13:41247168 | G | A | 22 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(19): Show |
27 | HG00544.hp1 HG00738.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.697+5477C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247168 | |||||||
| chr13:41247215 | C | T | 7 | a0001c0001t0003g0015 a0001c0001t0003g0033 a0001c0001t0003g0034 others(4): Show |
9 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.697+5430G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247215 | |||||||
| chr13:41247228 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0094 a0001c0001t0001g0123 others(3): Show |
7 | HG00423.hp2 NA18939.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.697+5417A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247228 | |||||||
| chr13:41247384 | A | G | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.697+5261T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247384 | |||||||
| chr13:41247605 | A | T | 2 | a0001c0006t0003g0016 a0001c0006t0003g0037 |
3 | HG02559.hp2 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.697+5040T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247605 | |||||||
| chr13:41247812 | G | GA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(3): Show |
10 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.697+4832dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247812 | |||||||
| chr13:41247889 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.697+4756T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41247889 | |||||||
| chr13:41248060 | C | T | 1 | a0001c0002t0001g0237 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.697+4585G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248060 | |||||||
| chr13:41248133 | T | C | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.697+4512A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248133 | |||||||
| chr13:41248166 | C | T | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.697+4479G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248166 | |||||||
| chr13:41248225 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.697+4420C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248225 | |||||||
| chr13:41248268 | C | T | 1 | a0001c0002t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.697+4377G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248268 | |||||||
| chr13:41248315 | T | C | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.697+4330A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248315 | |||||||
| chr13:41248634 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.697+4011G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248634 | |||||||
| chr13:41248652 | G | C | 4 | a0001c0002t0001g0184 a0001c0002t0001g0197 a0001c0002t0001g0198 others(1): Show |
4 | NA18939.hp2 NA18972.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+3993C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248652 | |||||||
| chr13:41248668 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.697+3977C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248668 | |||||||
| chr13:41248734 | C | T | 4 | a0001c0002t0001g0185 a0001c0002t0001g0186 a0001c0002t0001g0187 others(1): Show |
4 | HG02055.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+3911G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248734 | |||||||
| chr13:41248779 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.697+3866C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248779 | |||||||
| chr13:41248840 | A | G | 3 | a0001c0001t0001g0038 a0002c0008t0001g0265 a0002c0008t0001g0266 |
3 | HG01069.hp1 HG01071.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.697+3805T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248840 | |||||||
| chr13:41248842 | T | C | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+3803A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41248842 | |||||||
| chr13:41249094 | C | G | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.697+3551G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249094 | |||||||
| chr13:41249099 | CTA | C | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.697+3544_697+3545d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249099 | |||||||
| chr13:41249243 | A | G | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.697+3402T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249243 | |||||||
| chr13:41249264 | G | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0096 |
2 | HG01433.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.697+3381C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249264 | |||||||
| chr13:41249269 | C | T | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.697+3376G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249269 | |||||||
| chr13:41249289 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.697+3356G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249289 | |||||||
| chr13:41249294 | T | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0003g0015 others(6): Show |
11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.697+3351A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249294 | |||||||
| chr13:41249304 | G | A | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+3341C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249304 | |||||||
| chr13:41249619 | C | CT | 90 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(87): Show |
110 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.697+3025dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | |||||||
| chr13:41249619 | C | CTT | 45 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(42): Show |
53 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.697+3024_697+3025d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | |||||||
| chr13:41249619 | C | CTTT | 8 | a0001c0001t0001g0083 a0001c0001t0002g0044 a0001c0001t0002g0051 others(5): Show |
8 | HG01192.hp1 HG02135.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+3023_697+3025d others(5): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | |||||||
| chr13:41249619 | C | T | 3 | a0001c0001t0001g0038 a0005c0007t0001g0041 a0005c0007t0001g0042 |
3 | HG02622.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.697+3026G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | |||||||
| chr13:41249619 | CT | C | 85 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0048 others(82): Show |
116 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.697+3025delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | |||||||
| chr13:41249619 | CTTTTTT | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.697+3020_697+3025d others(8): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249619 | |||||||
| chr13:41249626 | T | C | 1 | a0001c0002t0001g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.697+3019A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249626 | |||||||
| chr13:41249628 | T | C | 6 | a0001c0002t0001g0028 a0001c0002t0001g0208 a0001c0002t0001g0217 others(3): Show |
7 | HG01261.hp2 HG01515.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.697+3017A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249628 | |||||||
| chr13:41249664 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.697+2981A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249664 | |||||||
| chr13:41249778 | T | C | 55 | a0001c0001t0001g0025 a0001c0001t0001g0143 a0001c0001t0001g0144 others(52): Show |
68 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.697+2867A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41249778 | |||||||
| chr13:41250165 | G | A | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.697+2480C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250165 | |||||||
| chr13:41250258 | T | C | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 |
3 | NA18967.hp2 NA19010.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.697+2387A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250258 | |||||||
| chr13:41250497 | A | T | 4 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0165 others(1): Show |
4 | HG01192.hp2 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.697+2148T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250497 | |||||||
| chr13:41250497 | AT | A | 11 | a0001c0001t0001g0047 a0001c0001t0001g0072 a0001c0001t0001g0131 others(8): Show |
11 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.697+2147delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250497 | |||||||
| chr13:41250527 | C | T | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.697+2118G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250527 | |||||||
| chr13:41250597 | G | T | 4 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0165 others(1): Show |
4 | HG01192.hp2 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.697+2048C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250597 | |||||||
| chr13:41250618 | C | T | 8 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(5): Show |
8 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.697+2027G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250618 | |||||||
| chr13:41250645 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.697+2000G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250645 | |||||||
| chr13:41250648 | C | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01070.hp1 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.697+1997G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250648 | |||||||
| chr13:41250699 | G | C | 1 | a0001c0001t0001g0134 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.697+1946C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250699 | |||||||
| chr13:41250700 | G | A | 1 | a0001c0002t0001g0200 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.697+1945C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250700 | |||||||
| chr13:41250731 | G | T | 1 | a0006c0011t0003g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.697+1914C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250731 | |||||||
| chr13:41250972 | A | G | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.697+1673T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41250972 | |||||||
| chr13:41251356 | T | C | 5 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.697+1289A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251356 | |||||||
| chr13:41251359 | C | T | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.697+1286G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251359 | |||||||
| chr13:41251404 | A | G | 1 | a0005c0007t0001g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.697+1241T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251404 | |||||||
| chr13:41251534 | A | G | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.697+1111T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251534 | |||||||
| chr13:41251609 | G | A | 9 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0003g0015 others(6): Show |
11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.697+1036C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251609 | |||||||
| chr13:41251728 | T | A | 12 | a0001c0002t0001g0012 a0001c0002t0001g0201 a0001c0002t0001g0202 others(9): Show |
14 | HG00558.hp2 HG02015.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.697+917A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251728 | |||||||
| chr13:41251929 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.697+716C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41251929 | |||||||
| chr13:41252114 | A | T | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.697+531T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41252114 | |||||||
| chr13:41252308 | T | TATAA | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.697+333_697+336dup others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41252308 | |||||||
| chr13:41252390 | C | A | 1 | a0001c0002t0002g0213 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.697+255G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41252390 | |||||||
| chr13:41252543 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.697+102T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 5/9 | chr13 | 41252543 | |||||||
| chr13:41252858 | C | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0048 |
3 | HG01884.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.589+91G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 4/9 | chr13 | 41252858 | |||||||
| chr13:41252905 | A | C | 2 | a0001c0002t0001g0230 a0001c0002t0001g0231 |
2 | HG02080.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.589+44T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 4/9 | chr13 | 41252905 | |||||||
| chr13:41253142 | T | C | 1 | a0001c0002t0001g0259 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.508-112A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253142 | |||||||
| chr13:41253340 | G | T | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.508-310C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253340 | |||||||
| chr13:41253342 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.508-312A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253342 | |||||||
| chr13:41253344 | A | G | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0032 others(10): Show |
15 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.508-314T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253344 | |||||||
| chr13:41253434 | T | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.508-404A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253434 | |||||||
| chr13:41253653 | A | T | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.508-623T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253653 | |||||||
| chr13:41253679 | G | C | 1 | a0001c0002t0001g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.508-649C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41253679 | |||||||
| chr13:41254091 | T | C | 21 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
26 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.507+438A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254091 | |||||||
| chr13:41254209 | CCTCTT | C | 16 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(13): Show |
21 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(18): Show |
intron_variant | MODIFIER | c.507+315_507+319del others(5): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254209 | |||||||
| chr13:41254250 | G | A | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.507+279C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254250 | |||||||
| chr13:41254293 | T | C | 1 | a0002c0003t0001g0174 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.507+236A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254293 | |||||||
| chr13:41254303 | C | T | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.507+226G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254303 | |||||||
| chr13:41254378 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+151T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254378 | |||||||
| chr13:41254507 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.507+22A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 3/9 | chr13 | 41254507 | |||||||
| chr13:41255034 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | NA19009.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.416-414T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255034 | |||||||
| chr13:41255354 | T | C | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-734A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255354 | |||||||
| chr13:41255388 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(11): Show |
20 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.416-768C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255388 | |||||||
| chr13:41255447 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.416-827A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255447 | |||||||
| chr13:41255466 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.416-846G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255466 | |||||||
| chr13:41255565 | G | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(116): Show |
142 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.416-945C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255565 | |||||||
| chr13:41255671 | G | A | 14 | a0002c0003t0001g0173 a0002c0003t0001g0174 a0002c0003t0004g0162 others(11): Show |
15 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.416-1051C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255671 | |||||||
| chr13:41255721 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.416-1101G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255721 | |||||||
| chr13:41255766 | G | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0003g0015 others(6): Show |
11 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-1146C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255766 | |||||||
| chr13:41255817 | C | A | 1 | a0001c0002t0001g0218 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.416-1197G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255817 | |||||||
| chr13:41255947 | C | T | 17 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(14): Show |
23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-1327G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255947 | |||||||
| chr13:41255960 | T | A | 19 | a0002c0003t0001g0173 a0002c0003t0001g0174 a0002c0003t0004g0162 others(16): Show |
20 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.416-1340A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41255960 | |||||||
| chr13:41256124 | C | G | 123 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(120): Show |
146 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.416-1504G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256124 | |||||||
| chr13:41256328 | AT | A | 150 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
182 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.416-1709delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256328 | |||||||
| chr13:41256350 | G | A | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-1730C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256350 | |||||||
| chr13:41256387 | T | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.416-1767A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256387 | |||||||
| chr13:41256388 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.416-1768C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256388 | |||||||
| chr13:41256614 | G | A | 5 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-1994C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256614 | |||||||
| chr13:41256622 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.416-2002G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256622 | |||||||
| chr13:41256654 | CCA | C | 8 | a0001c0001t0001g0032 a0001c0001t0003g0015 a0001c0001t0003g0033 others(5): Show |
10 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-2036_416-2035d others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256654 | |||||||
| chr13:41256741 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.416-2121G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256741 | |||||||
| chr13:41256770 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-2150C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256770 | |||||||
| chr13:41256808 | T | C | 2 | a0002c0003t0001g0173 a0002c0003t0001g0174 |
2 | HG01981.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.416-2188A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256808 | |||||||
| chr13:41256826 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.416-2206A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256826 | |||||||
| chr13:41256906 | G | A | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.416-2286C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256906 | |||||||
| chr13:41256976 | A | G | 17 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(14): Show |
23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-2356T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41256976 | |||||||
| chr13:41257125 | A | G | 1 | a0001c0002t0001g0178 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.416-2505T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257125 | |||||||
| chr13:41257134 | G | A | 3 | a0001c0001t0005g0160 a0001c0002t0001g0217 a0001c0002t0001g0218 |
3 | HG01261.hp2 HG01516.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.416-2514C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257134 | |||||||
| chr13:41257335 | A | T | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.416-2715T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257335 | |||||||
| chr13:41257508 | A | C | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.416-2888T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257508 | |||||||
| chr13:41257720 | T | G | 1 | a0002c0003t0004g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.415+2773A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257720 | |||||||
| chr13:41257909 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.415+2584G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41257909 | |||||||
| chr13:41258147 | T | C | 3 | a0004c0005t0001g0026 a0004c0005t0001g0175 a0004c0005t0001g0176 |
4 | HG01109.hp1 HG01192.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+2346A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258147 | |||||||
| chr13:41258224 | G | A | 17 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(14): Show |
23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+2269C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258224 | |||||||
| chr13:41258404 | C | T | 1 | a0001c0002t0001g0178 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.415+2089G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258404 | |||||||
| chr13:41258498 | G | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.415+1995C>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258498 | |||||||
| chr13:41258569 | A | C | 1 | a0006c0011t0003g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.415+1924T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258569 | |||||||
| chr13:41258574 | A | C | 9 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(6): Show |
14 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.415+1919T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258574 | |||||||
| chr13:41258575 | C | A | 18 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(15): Show |
24 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.415+1918G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258575 | |||||||
| chr13:41258575 | CA | C | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
158 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.415+1917delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258575 | |||||||
| chr13:41258576 | A | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(15): Show |
24 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.415+1917T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258576 | |||||||
| chr13:41258577 | A | AAC | 18 | a0002c0003t0001g0173 a0002c0003t0001g0174 a0002c0003t0004g0162 others(15): Show |
19 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.415+1915_415+1916i others(4): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258577 | |||||||
| chr13:41258577 | A | T | 2 | a0001c0002t0001g0226 a0001c0002t0001g0227 |
2 | HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.415+1916T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258577 | |||||||
| chr13:41258870 | A | T | 8 | a0001c0001t0001g0032 a0001c0001t0003g0015 a0001c0001t0003g0033 others(5): Show |
10 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+1623T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258870 | |||||||
| chr13:41258928 | A | T | 1 | a0001c0001t0002g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.415+1565T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41258928 | |||||||
| chr13:41259121 | T | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.415+1372A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259121 | |||||||
| chr13:41259131 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA18955.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.415+1362G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259131 | |||||||
| chr13:41259203 | C | G | 17 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(14): Show |
23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+1290G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259203 | |||||||
| chr13:41259205 | A | G | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.415+1288T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259205 | |||||||
| chr13:41259209 | C | G | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.415+1284G>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259209 | |||||||
| chr13:41259273 | T | A | 1 | a0001c0002t0001g0219 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.415+1220A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259273 | |||||||
| chr13:41259432 | G | A | 5 | a0003c0004t0001g0167 a0003c0004t0001g0169 a0003c0004t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+1061C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259432 | |||||||
| chr13:41259463 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(4): Show |
8 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1030C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259463 | |||||||
| chr13:41259487 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.415+1006T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259487 | |||||||
| chr13:41259541 | A | C | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.415+952T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259541 | |||||||
| chr13:41259619 | G | A | 1 | a0006c0011t0003g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.415+874C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259619 | |||||||
| chr13:41259701 | C | CA | 10 | a0001c0002t0001g0220 a0001c0002t0001g0221 a0001c0002t0001g0254 others(7): Show |
10 | HG00280.hp2 HG01952.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+791dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259701 | |||||||
| chr13:41259701 | C | CAA | 9 | a0002c0003t0004g0165 a0002c0003t0004g0166 a0002c0008t0001g0265 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.415+790_415+791dup others(2): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259701 | |||||||
| chr13:41259701 | C | CAAAAAAA others(14): Show |
9 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(6): Show |
14 | HG02165.hp2 NA18952.hp1 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.415+791_415+792ins others(21): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259701 | |||||||
| chr13:41259701 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0002g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.415+791_415+792ins others(21): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259701 | |||||||
| chr13:41259702 | A | AAAAAAAA others(15): Show |
8 | a0001c0001t0001g0032 a0001c0001t0003g0015 a0001c0001t0003g0033 others(5): Show |
10 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+790_415+791ins others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259702 | |||||||
| chr13:41259702 | A | AAAAAAAC others(16): Show |
113 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.415+790_415+791ins others(23): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259702 | |||||||
| chr13:41259712 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.415+780_415+781ins others(24): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | |||||||
| chr13:41259712 | A | AAAAAAAA others(18): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0039 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.415+780_415+781ins others(25): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | |||||||
| chr13:41259712 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.415+780_415+781ins others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | |||||||
| chr13:41259712 | A | AAAAAAAA others(17): Show |
2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.415+780_415+781ins others(24): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | |||||||
| chr13:41259712 | A | AAAAAAAC others(14): Show |
6 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.415+780_415+781ins others(21): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | |||||||
| chr13:41259712 | A | AAAAAACA others(15): Show |
1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.415+780_415+781ins others(22): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | |||||||
| chr13:41259712 | A | C | 131 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
159 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.415+781T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259712 | |||||||
| chr13:41259785 | A | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.415+708T>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259785 | |||||||
| chr13:41259865 | G | A | 1 | a0001c0002t0001g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.415+628C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41259865 | |||||||
| chr13:41260057 | G | A | 4 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0225 others(1): Show |
4 | HG00558.hp2 NA18953.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+436C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260057 | |||||||
| chr13:41260123 | A | G | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.415+370T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260123 | |||||||
| chr13:41260220 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.415+273G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260220 | |||||||
| chr13:41260221 | G | T | 5 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+272C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260221 | |||||||
| chr13:41260271 | G | A | 1 | a0001c0002t0001g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415+222C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260271 | |||||||
| chr13:41260442 | G | GT | 11 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0051 others(8): Show |
16 | HG02165.hp2 NA18952.hp1 NA18953.hp1 others(13): Show |
intron_variant | MODIFIER | c.415+50dupA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260442 | |||||||
| chr13:41260442 | GT | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(108): Show |
132 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.415+50delA | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 2/9 | chr13 | 41260442 | |||||||
| chr13:41260940 | T | TA | 167 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-8-26dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41260940 | |||||||
| chr13:41260953 | T | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-8-38A>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41260953 | |||||||
| chr13:41260970 | A | G | 61 | a0001c0002t0001g0002 a0001c0002t0001g0011 a0001c0002t0001g0012 others(58): Show |
73 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-8-55T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41260970 | |||||||
| chr13:41261210 | T | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02080.hp2 HG02165.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-8-295A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261210 | |||||||
| chr13:41261269 | G | A | 19 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
25 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-354C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261269 | |||||||
| chr13:41261370 | CATAATTC others(2): Show |
C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-8-464_-8-456delAA others(7): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261370 | |||||||
| chr13:41261593 | C | T | 13 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(10): Show |
13 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-678G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261593 | |||||||
| chr13:41261676 | A | G | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8-761T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261676 | |||||||
| chr13:41261988 | T | C | 1 | a0006c0011t0003g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-8-1073A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261988 | |||||||
| chr13:41261990 | T | TA | 124 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(121): Show |
146 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-8-1076dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261990 | |||||||
| chr13:41261990 | T | TAA | 44 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
56 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.-8-1077_-8-1076dup others(2): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41261990 | |||||||
| chr13:41262036 | T | A | 1 | a0001c0002t0001g0259 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-8-1121A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262036 | |||||||
| chr13:41262061 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-8-1146C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262061 | |||||||
| chr13:41262075 | G | A | 2 | a0005c0007t0001g0041 a0005c0007t0001g0042 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-8-1160C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262075 | |||||||
| chr13:41262093 | T | C | 112 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(109): Show |
133 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-8-1178A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262093 | |||||||
| chr13:41262103 | G | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
145 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.-8-1188C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262103 | |||||||
| chr13:41262107 | C | T | 19 | a0002c0003t0001g0173 a0002c0003t0001g0174 a0002c0003t0004g0162 others(16): Show |
20 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-1192G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262107 | |||||||
| chr13:41262193 | A | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(4): Show |
8 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-1278T>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262193 | |||||||
| chr13:41262328 | C | T | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-9+1157G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262328 | |||||||
| chr13:41262338 | C | CA | 106 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(103): Show |
125 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-9+1146dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262338 | |||||||
| chr13:41262338 | C | CAA | 13 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
15 | HG01346.hp2 HG02071.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+1145_-9+1146dup others(2): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262338 | |||||||
| chr13:41262338 | CA | C | 6 | a0002c0003t0004g0162 a0002c0003t0004g0163 a0002c0003t0004g0164 others(3): Show |
6 | HG00280.hp2 HG01192.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1146delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262338 | |||||||
| chr13:41262338 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9+1135_-9+1146del others(12): Show |
MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262338 | |||||||
| chr13:41262351 | A | G | 1 | a0006c0011t0003g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-9+1134T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262351 | |||||||
| chr13:41262358 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-9+1127C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262358 | |||||||
| chr13:41262358 | GA | G | 15 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
21 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+1126delT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262358 | |||||||
| chr13:41262359 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+1126T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262359 | |||||||
| chr13:41262467 | G | T | 1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-9+1018C>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262467 | |||||||
| chr13:41262644 | G | GA | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-9+840dupT | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262644 | |||||||
| chr13:41262689 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-9+796T>C | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262689 | |||||||
| chr13:41262968 | G | A | 2 | a0002c0008t0001g0265 a0002c0008t0001g0266 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-9+517C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262968 | |||||||
| chr13:41262990 | G | A | 17 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0046 others(14): Show |
23 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-9+495C>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41262990 | |||||||
| chr13:41263019 | T | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
134 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-9+466A>G | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41263019 | |||||||
| chr13:41263068 | C | A | 1 | a0001c0002t0001g0267 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-9+417G>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41263068 | |||||||
| chr13:41263084 | C | T | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-9+401G>A | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41263084 | |||||||
| chr13:41263476 | T | A | 1 | a0001c0001t0001g0268 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-9+9A>T | MTRF1 | ENSG00000120662.16 | transcript | ENST00000379480.9 | protein_coding | 1/9 | chr13 | 41263476 |