Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51507 |
| ensemblid | ENSG00000022277.13 |
| hgncid | 15890 |
| symbol | RTF2 |
| name | replication termination factor 2 |
| refseq_nuc | NM_016407.5 |
| refseq_prot | NP_057491.2 |
| ensembl_nuc | ENST00000357348.10 |
| ensembl_prot | ENSP00000349906.6 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 56468627 |
| end | 56519449 |
| strand | + |
| ver | v1.2 |
| region | chr20:56468627-56519449 |
| region5000 | chr20:56463627-56524449 |
| regionname0 | RTF2_chr20_56468627_56519449 |
| regionname5000 | RTF2_chr20_56463627_56524449 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 306 | 348 | 77 | 59 | 173 | 8 | 30 | 133 | RTF2_chr20_56463627_56524449 | RTF2 | MGCDG others(301): Show |
chr20 | 56463627 | 56524449 |
| a0002 | 1/0 | 306 | 39 | 11 | 9 | 3 | 6 | 9 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | MGCDG others(301): Show |
chr20 | 56463627 | 56524449 |
| a0003 | 0/0 | 306 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | MGCDG others(301): Show |
chr20 | 56463627 | 56524449 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 918 | 339 | 73 | 58 | 172 | 8 | 27 | RTF2_chr20_56463627_56524449 | RTF2 | ATGGG others(913): Show |
chr20 | 56463627 | 56524449 | ||
| a0001c0003 | 0/0 | 918 | 4 | 4 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | ATGGG others(913): Show |
chr20 | 56463627 | 56524449 | ||
| a0001c0004 | 0/0 | 918 | 3 | 0 | 0 | 1 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | ATGGG others(913): Show |
chr20 | 56463627 | 56524449 | ||
| a0001c0006 | 0/0 | 918 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | ATGGG others(913): Show |
chr20 | 56463627 | 56524449 | ||
| a0001c0007 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | ATGGG others(913): Show |
chr20 | 56463627 | 56524449 | ||
| a0002c0002 | 1/0 | 918 | 38 | 11 | 9 | 3 | 6 | 8 | RTF2_chr20_56463627_56524449 | RTF2 | ATGGG others(913): Show |
chr20 | 56463627 | 56524449 | ||
| a0002c0008 | 0/0 | 918 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | ATGGG others(913): Show |
chr20 | 56463627 | 56524449 | ||
| a0003c0005 | 0/0 | 918 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | ATGGG others(913): Show |
chr20 | 56463627 | 56524449 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2176 | 236 | 46 | 28 | 150 | 2 | 10 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0001t0002 | 0/1 | 2176 | 88 | 25 | 26 | 15 | 6 | 15 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0001t0003 | 0/0 | 2168 | 5 | 0 | 0 | 5 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2163): Show |
chr20 | 56463627 | 56524449 |
| a0001c0001t0004 | 0/0 | 2176 | 3 | 0 | 3 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0001t0005 | 0/0 | 2176 | 2 | 0 | 0 | 0 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0001t0006 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0001t0007 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0001t0008 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0001t0009 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0001t0010 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0003t0002 | 0/0 | 2176 | 4 | 4 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0004t0002 | 0/0 | 2176 | 3 | 0 | 0 | 1 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0006t0001 | 0/0 | 2176 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0001c0007t0001 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0002c0002t0001 | 1/0 | 2176 | 37 | 11 | 8 | 3 | 6 | 8 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0002c0002t0002 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0002c0008t0001 | 0/0 | 2176 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| a0003c0005t0001 | 0/0 | 2176 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | GCGGA others(2171): Show |
chr20 | 56463627 | 56524449 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 4 | 1 | 1 | 5 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0041 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0001t0010g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0003t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0004t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0004t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0001c0007t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0228 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0002c0008t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| a0003c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | FIN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0233 | EUR | FIN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00738 | hp1 | a0001 | c0007 | t0001 | g0053 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0242 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0216 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0166 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0250 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0203 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02080 | hp1 | a0001 | c0004 | t0002 | g0038 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0224 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | CDX | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CDX | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0130 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0255 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0246 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0113 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0254 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02897 | hp1 | a0001 | c0003 | t0002 | g0253 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0235 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0172 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0232 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0252 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0238 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0227 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03704 | hp2 | a0003 | c0005 | t0001 | g0229 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0114 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0239 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03834 | hp1 | a0002 | c0008 | t0001 | g0226 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03927 | hp1 | a0001 | c0004 | t0002 | g0014 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0048 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0236 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG04184 | hp1 | a0001 | c0006 | t0001 | g0095 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | YRI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | CHB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0118 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ASW | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ASW | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0248 | EUR | TSI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | TSI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0241 | EUR | TSI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20905 | hp1 | a0001 | c0004 | t0002 | g0014 | SAS | GIH | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | USA | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | USA | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | USA | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | USA | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0206 | REF | REF | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0228 | REF | REF | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:56473304 | G | A | 1 | a0003 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.73G>A | p.Asp25Asn | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/9 | 144/2176 | 73/921 | 25/306 | chr20 | 56473304 | |||
| chr20:56513348 | A | G | 1 | a0001 | 347 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(344): Show |
missense_variant | MODERATE | c.511A>G | p.Met171Val | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/9 | 582/2176 | 511/921 | 171/306 | chr20 | 56513348 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:56477059 | C | T | 1 | a0001c0004 | 3 | HG02080.hp1 HG03927.hp1 NA20905.hp1 |
synonymous_variant | LOW | c.333C>T | p.His111His | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/9 | 404/2176 | 333/921 | 111/306 | chr20 | 56477059 | |||
| chr20:56477092 | C | T | 1 | a0002c0008 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.366C>T | p.Pro122Pro | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/9 | 437/2176 | 366/921 | 122/306 | chr20 | 56477092 | |||
| chr20:56477113 | C | T | 1 | a0001c0007 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.387C>T | p.Asn129Asn | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/9 | 458/2176 | 387/921 | 129/306 | chr20 | 56477113 | |||
| chr20:56484132 | C | T | 1 | a0001c0003 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.420C>T | p.Cys140Cys | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/9 | 491/2176 | 420/921 | 140/306 | chr20 | 56484132 | |||
| chr20:56513377 | C | T | 1 | a0001c0006 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.540C>T | p.Asp180Asp | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/9 | 611/2176 | 540/921 | 180/306 | chr20 | 56513377 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:56468643 | A | G | 1 | a0001c0001t0010 | 1 | HG01175.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/9 | 55 | chr20 | 56468643 | ||||||
| chr20:56468643 | A | T | 1 | a0001c0001t0004 | 3 | HG01074.hp1 HG01167.hp2 HG01952.hp2 |
5_prime_UTR_variant | MODIFIER | c.-55A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/9 | 55 | chr20 | 56468643 | ||||||
| chr20:56518372 | TGTCATAA others(1): Show |
T | 1 | a0001c0001t0003 | 5 | HG00609.hp2 NA18952.hp1 NA18967.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*116delTCATAA others(2): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 109 | INFO_REALIGN_3_PRIME | chr20 | 56518372 | |||||
| chr20:56518381 | G | C | 1 | a0001c0001t0003 | 5 | HG00609.hp2 NA18952.hp1 NA18967.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*116G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 116 | chr20 | 56518381 | ||||||
| chr20:56518385 | T | G | 1 | a0001c0001t0003 | 5 | HG00609.hp2 NA18952.hp1 NA18967.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*120T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 120 | chr20 | 56518385 | ||||||
| chr20:56518405 | G | A | 1 | a0001c0001t0010 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*140G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 140 | chr20 | 56518405 | ||||||
| chr20:56518572 | C | T | 1 | a0001c0001t0009 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 307 | chr20 | 56518572 | ||||||
| chr20:56518602 | A | G | 1 | a0001c0001t0008 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 337 | chr20 | 56518602 | ||||||
| chr20:56518641 | A | G | 1 | a0001c0001t0010 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*376A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 376 | chr20 | 56518641 | ||||||
| chr20:56518845 | A | G | 4 | a0001c0001t0002 a0001c0003t0002 a0001c0004t0002 others(1): Show |
95 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*580A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 580 | chr20 | 56518845 | ||||||
| chr20:56518934 | C | A | 1 | a0001c0001t0005 | 2 | HG02735.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*669C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 669 | chr20 | 56518934 | ||||||
| chr20:56518943 | C | T | 1 | a0001c0001t0008 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*678C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 678 | chr20 | 56518943 | ||||||
| chr20:56519410 | C | G | 1 | a0001c0001t0007 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 1145 | chr20 | 56519410 | ||||||
| chr20:56519441 | T | C | 1 | a0001c0001t0006 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1176T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 1176 | chr20 | 56519441 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:56469127 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(35): Show |
50 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.69+361C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469127 | |||||||
| chr20:56469141 | C | G | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+375C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469141 | |||||||
| chr20:56469783 | ATCT | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
249 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.69+1021_69+1023del others(3): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56469783 | ||||||
| chr20:56469784 | T | G | 1 | a0001c0001t0002g0001 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.69+1018T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469784 | |||||||
| chr20:56469813 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0175 |
3 | NA18946.hp2 NA18959.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.69+1047T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469813 | |||||||
| chr20:56469867 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.69+1101C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469867 | |||||||
| chr20:56469880 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.69+1114C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469880 | |||||||
| chr20:56469946 | A | G | 1 | a0001c0001t0002g0250 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.69+1180A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469946 | |||||||
| chr20:56470047 | C | G | 1 | a0001c0001t0002g0249 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.69+1281C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470047 | |||||||
| chr20:56470108 | G | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(255): Show |
349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.69+1342G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470108 | |||||||
| chr20:56470140 | A | G | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+1374A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470140 | |||||||
| chr20:56470170 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+1404G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470170 | |||||||
| chr20:56470207 | C | A | 1 | a0002c0002t0001g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.69+1441C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470207 | |||||||
| chr20:56470318 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.69+1552C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470318 | |||||||
| chr20:56470369 | A | T | 1 | a0001c0001t0001g0034 | 2 | NA19004.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.69+1603A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470369 | |||||||
| chr20:56470448 | C | T | 7 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(4): Show |
10 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+1682C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470448 | |||||||
| chr20:56470493 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(34): Show |
48 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.69+1727G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470493 | |||||||
| chr20:56470576 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
259 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.69+1810G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470576 | |||||||
| chr20:56470696 | T | C | 7 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(4): Show |
10 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+1930T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470696 | |||||||
| chr20:56470787 | T | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(134): Show |
186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.69+2021T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470787 | |||||||
| chr20:56471002 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.69+2236G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471002 | |||||||
| chr20:56471003 | A | G | 26 | a0002c0002t0001g0017 a0002c0002t0001g0044 a0002c0002t0001g0045 others(23): Show |
33 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.69+2237A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471003 | |||||||
| chr20:56471097 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.70-2204G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471097 | |||||||
| chr20:56471339 | C | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG01261.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.70-1962C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471339 | |||||||
| chr20:56471427 | G | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
82 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.70-1874G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471427 | |||||||
| chr20:56471548 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.70-1753A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471548 | |||||||
| chr20:56471563 | G | C | 1 | a0001c0007t0001g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.70-1738G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471563 | |||||||
| chr20:56471566 | T | TCAAAA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0163 a0001c0001t0001g0164 others(9): Show |
15 | HG01175.hp1 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.70-1734_70-1730dup others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56471566 | ||||||
| chr20:56471566 | T | TCAAAACA others(3): Show |
2 | a0001c0001t0001g0165 a0001c0007t0001g0053 |
2 | HG00738.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.70-1730_70-1729ins others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56471566 | ||||||
| chr20:56471572 | A | AAAAAC | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
185 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.70-1713_70-1709dup others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56471572 | ||||||
| chr20:56471572 | A | AAAAC | 7 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(4): Show |
10 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-1726_70-1725ins others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56471572 | ||||||
| chr20:56471572 | A | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(54): Show |
71 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.70-1729A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471572 | |||||||
| chr20:56471597 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.70-1704T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471597 | |||||||
| chr20:56471679 | T | C | 57 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0009 others(54): Show |
81 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.70-1622T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471679 | |||||||
| chr20:56471844 | G | C | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-1457G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471844 | |||||||
| chr20:56471990 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
340 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.70-1311C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471990 | |||||||
| chr20:56472170 | G | A | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.70-1131G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472170 | |||||||
| chr20:56472183 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0175 others(1): Show |
8 | HG00544.hp2 NA18612.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-1118T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472183 | |||||||
| chr20:56472196 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.70-1105G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472196 | |||||||
| chr20:56472576 | T | TA | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
250 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.70-715dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56472576 | ||||||
| chr20:56472624 | C | T | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0288 |
3 | HG01891.hp2 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.70-677C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472624 | |||||||
| chr20:56472627 | A | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-674A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472627 | |||||||
| chr20:56472873 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
187 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.70-428C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472873 | |||||||
| chr20:56472959 | C | T | 2 | a0001c0001t0005g0113 a0001c0001t0005g0114 |
2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.70-342C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472959 | |||||||
| chr20:56473226 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70-75T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56473226 | |||||||
| chr20:56473227 | A | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
187 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.70-74A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56473227 | |||||||
| chr20:56473236 | T | G | 1 | a0001c0001t0001g0043 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.70-65T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56473236 | |||||||
| chr20:56473440 | T | TGAG | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
346 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.164+46_164+48dupGA others(1): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 56473440 | ||||||
| chr20:56473688 | A | G | 1 | a0002c0002t0001g0248 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.164+293A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56473688 | |||||||
| chr20:56473708 | A | AC | 2 | a0001c0001t0001g0008 a0001c0001t0001g0173 |
5 | HG02145.hp1 HG02976.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+317dupC | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 56473708 | ||||||
| chr20:56473770 | C | A | 1 | a0001c0001t0002g0037 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.164+375C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56473770 | |||||||
| chr20:56474014 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.164+619T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474014 | |||||||
| chr20:56474030 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164+635C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474030 | |||||||
| chr20:56474092 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
350 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.165-586A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474092 | |||||||
| chr20:56474353 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.165-325C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474353 | |||||||
| chr20:56474373 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.165-305C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474373 | |||||||
| chr20:56474413 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.165-265G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474413 | |||||||
| chr20:56474432 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.165-246G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474432 | |||||||
| chr20:56474524 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165-154A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474524 | |||||||
| chr20:56474588 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02027.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.165-90C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474588 | |||||||
| chr20:56474852 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
251 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.258+81A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56474852 | |||||||
| chr20:56475043 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.258+272T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475043 | |||||||
| chr20:56475280 | A | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
252 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.258+509A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475280 | |||||||
| chr20:56475331 | A | G | 1 | a0002c0002t0001g0247 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.258+560A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475331 | |||||||
| chr20:56475519 | G | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG01261.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.258+748G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475519 | |||||||
| chr20:56475547 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.258+776T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475547 | |||||||
| chr20:56475599 | C | T | 1 | a0001c0001t0008g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.258+828C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475599 | |||||||
| chr20:56475666 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.258+895A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475666 | |||||||
| chr20:56475667 | T | C | 1 | a0002c0002t0001g0230 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.258+896T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475667 | |||||||
| chr20:56475681 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.258+910T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475681 | |||||||
| chr20:56475876 | C | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
251 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.258+1105C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475876 | |||||||
| chr20:56476069 | T | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(34): Show |
48 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.259-916T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476069 | |||||||
| chr20:56476168 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.259-817C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476168 | |||||||
| chr20:56476252 | A | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(35): Show |
49 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.259-733A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476252 | |||||||
| chr20:56476301 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(45): Show |
62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.259-684G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476301 | |||||||
| chr20:56476401 | T | A | 1 | a0001c0001t0002g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.259-584T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476401 | |||||||
| chr20:56476461 | T | C | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-524T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476461 | |||||||
| chr20:56476475 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.259-510A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476475 | |||||||
| chr20:56476502 | C | CT | 110 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(107): Show |
151 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.259-469dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 56476502 | ||||||
| chr20:56476502 | C | CTT | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
196 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.259-470_259-469dup others(2): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 56476502 | ||||||
| chr20:56476622 | C | T | 1 | a0002c0002t0002g0216 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.259-363C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476622 | |||||||
| chr20:56476688 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.259-297G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476688 | |||||||
| chr20:56476699 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.259-286A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476699 | |||||||
| chr20:56476750 | C | T | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.259-235C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476750 | |||||||
| chr20:56476795 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-190G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476795 | |||||||
| chr20:56476797 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(125): Show |
176 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.259-188C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476797 | |||||||
| chr20:56476917 | T | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(46): Show |
63 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.259-68T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476917 | |||||||
| chr20:56477221 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.398+97C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477221 | |||||||
| chr20:56477291 | G | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(46): Show |
63 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.398+167G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477291 | |||||||
| chr20:56477363 | CAA | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0109 a0001c0001t0001g0116 |
4 | HG01123.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+242_398+243del others(2): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56477363 | ||||||
| chr20:56477550 | TC | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.398+428delC | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56477550 | ||||||
| chr20:56477653 | G | C | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.398+529G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477653 | |||||||
| chr20:56477905 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.398+781A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477905 | |||||||
| chr20:56477909 | A | G | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0288 |
3 | HG01891.hp2 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.398+785A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477909 | |||||||
| chr20:56477937 | A | T | 1 | a0001c0001t0002g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.398+813A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477937 | |||||||
| chr20:56477952 | T | A | 1 | a0001c0001t0001g0019 | 2 | NA18947.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.398+828T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477952 | |||||||
| chr20:56478006 | G | A | 2 | a0002c0002t0001g0231 a0002c0002t0001g0232 |
2 | HG02683.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.398+882G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478006 | |||||||
| chr20:56478126 | G | A | 4 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0186 others(1): Show |
4 | HG01978.hp2 HG03942.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.398+1002G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478126 | |||||||
| chr20:56478162 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.398+1038G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478162 | |||||||
| chr20:56478401 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.398+1277A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478401 | |||||||
| chr20:56478412 | T | C | 1 | a0001c0001t0002g0037 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.398+1288T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478412 | |||||||
| chr20:56478636 | T | C | 1 | a0001c0007t0001g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.398+1512T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478636 | |||||||
| chr20:56478762 | T | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
346 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.398+1638T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478762 | |||||||
| chr20:56478810 | G | A | 4 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0186 others(1): Show |
4 | HG01978.hp2 HG03942.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.398+1686G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478810 | |||||||
| chr20:56478936 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.398+1812A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478936 | |||||||
| chr20:56479094 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(5): Show |
11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.398+1970G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479094 | |||||||
| chr20:56479248 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
187 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.398+2124C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479248 | |||||||
| chr20:56479251 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.398+2127A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479251 | |||||||
| chr20:56479294 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(45): Show |
62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.398+2170C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479294 | |||||||
| chr20:56479330 | AT | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(45): Show |
62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.398+2208delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479330 | ||||||
| chr20:56479346 | G | A | 1 | a0001c0001t0004g0020 | 2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.398+2222G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479346 | |||||||
| chr20:56479380 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.398+2256C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479380 | |||||||
| chr20:56479520 | G | A | 1 | a0002c0002t0001g0233 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.398+2396G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479520 | |||||||
| chr20:56479558 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.398+2434G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479558 | |||||||
| chr20:56479784 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(38): Show |
65 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.398+2660C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479784 | |||||||
| chr20:56479818 | C | CT | 79 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(76): Show |
113 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.398+2712dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479818 | ||||||
| chr20:56479818 | C | CTT | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
7 | HG02015.hp1 NA18612.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.398+2711_398+2712d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479818 | ||||||
| chr20:56479818 | CT | C | 8 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0013 others(5): Show |
11 | HG02258.hp2 HG02647.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.398+2712delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479818 | ||||||
| chr20:56479818 | CTTTTTTT others(4): Show |
C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
189 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.398+2702_398+2712d others(13): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479818 | ||||||
| chr20:56479852 | A | G | 1 | a0001c0001t0002g0016 | 3 | HG01109.hp2 HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.398+2728A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479852 | |||||||
| chr20:56479854 | G | A | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.398+2730G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479854 | |||||||
| chr20:56480099 | C | G | 1 | a0001c0001t0002g0037 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.398+2975C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480099 | |||||||
| chr20:56480121 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.398+2997C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480121 | |||||||
| chr20:56480181 | A | G | 2 | a0001c0001t0002g0212 a0001c0001t0002g0213 |
2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.398+3057A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480181 | |||||||
| chr20:56480265 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.398+3141C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480265 | |||||||
| chr20:56480311 | C | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
345 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.398+3187C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480311 | |||||||
| chr20:56480536 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.398+3412C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480536 | |||||||
| chr20:56481179 | C | G | 2 | a0001c0001t0002g0189 a0001c0001t0002g0211 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.399-2932C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481179 | |||||||
| chr20:56481211 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.399-2900C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481211 | |||||||
| chr20:56481213 | C | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.399-2898C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481213 | |||||||
| chr20:56481345 | G | A | 1 | a0002c0002t0001g0234 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.399-2766G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481345 | |||||||
| chr20:56481357 | G | C | 1 | a0002c0002t0001g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.399-2754G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481357 | |||||||
| chr20:56481492 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0060 a0001c0001t0001g0061 |
4 | HG00733.hp1 HG01081.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.399-2619G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481492 | |||||||
| chr20:56481533 | A | G | 57 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(54): Show |
81 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.399-2578A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481533 | |||||||
| chr20:56481628 | CAT | C | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(47): Show |
64 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.399-2479_399-2478d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56481628 | ||||||
| chr20:56481754 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.399-2357G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481754 | |||||||
| chr20:56481883 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.399-2228C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481883 | |||||||
| chr20:56481923 | A | T | 1 | a0001c0001t0001g0271 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.399-2188A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481923 | |||||||
| chr20:56481971 | A | C | 1 | a0001c0001t0002g0177 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.399-2140A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481971 | |||||||
| chr20:56482144 | T | G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0063 others(2): Show |
7 | HG00597.hp2 NA18941.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.399-1967T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482144 | |||||||
| chr20:56482158 | G | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(76): Show |
102 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.399-1953G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482158 | |||||||
| chr20:56482333 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.399-1778A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482333 | |||||||
| chr20:56482342 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(134): Show |
186 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.399-1769A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482342 | |||||||
| chr20:56482356 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.399-1755G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482356 | |||||||
| chr20:56482404 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.399-1707C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482404 | |||||||
| chr20:56482480 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.399-1631C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482480 | |||||||
| chr20:56482673 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
5 | HG00438.hp1 HG02056.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.399-1438C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482673 | |||||||
| chr20:56482831 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.399-1280C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482831 | |||||||
| chr20:56482848 | G | A | 58 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(55): Show |
82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.399-1263G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482848 | |||||||
| chr20:56482858 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.399-1253G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482858 | |||||||
| chr20:56482864 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.399-1247T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482864 | |||||||
| chr20:56482937 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.399-1174C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482937 | |||||||
| chr20:56483239 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.399-872T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56483239 | |||||||
| chr20:56483341 | C | CT | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(136): Show |
188 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.399-756dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56483341 | ||||||
| chr20:56483343 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.399-768T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56483343 | |||||||
| chr20:56483752 | T | C | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.399-359T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56483752 | |||||||
| chr20:56483916 | CT | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0133 |
4 | NA18940.hp1 NA18941.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.399-187delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56483916 | ||||||
| chr20:56484342 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.477+153C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484342 | |||||||
| chr20:56484605 | C | T | 1 | a0001c0001t0007g0118 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.477+416C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484605 | |||||||
| chr20:56484795 | A | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+606A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484795 | |||||||
| chr20:56484854 | A | G | 5 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0186 others(2): Show |
5 | HG01256.hp2 HG01978.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+665A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484854 | |||||||
| chr20:56484893 | T | TG | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
350 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.477+704_477+705ins others(1): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484893 | |||||||
| chr20:56485199 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.477+1010G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485199 | |||||||
| chr20:56485250 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+1061G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485250 | |||||||
| chr20:56485565 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.477+1376G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485565 | |||||||
| chr20:56485709 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.477+1520T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485709 | |||||||
| chr20:56485822 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.477+1633G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485822 | |||||||
| chr20:56486127 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+1938C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486127 | |||||||
| chr20:56486195 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.477+2006G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486195 | |||||||
| chr20:56486275 | T | C | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+2086T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486275 | |||||||
| chr20:56486318 | A | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0108 |
2 | HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.477+2129A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486318 | |||||||
| chr20:56486524 | C | G | 1 | a0003c0005t0001g0229 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.477+2335C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486524 | |||||||
| chr20:56486656 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0069 |
3 | NA19003.hp2 NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.477+2467T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486656 | |||||||
| chr20:56486850 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0121 a0001c0001t0001g0122 |
4 | HG01884.hp2 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.477+2661G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486850 | |||||||
| chr20:56486852 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
350 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.477+2663A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486852 | |||||||
| chr20:56487005 | A | G | 1 | a0001c0001t0002g0042 | 2 | HG00642.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.477+2816A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487005 | |||||||
| chr20:56487021 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.477+2832A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487021 | |||||||
| chr20:56487147 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
7 | NA18953.hp2 NA18960.hp1 NA19065.hp1 others(4): Show |
intron_variant | MODIFIER | c.477+2958G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487147 | |||||||
| chr20:56487180 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(77): Show |
103 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.477+2991A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487180 | |||||||
| chr20:56487216 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.477+3027C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487216 | |||||||
| chr20:56487281 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+3092A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487281 | |||||||
| chr20:56487390 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+3201C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487390 | |||||||
| chr20:56487391 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.477+3202G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487391 | |||||||
| chr20:56487438 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(134): Show |
186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.477+3249G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487438 | |||||||
| chr20:56487477 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0219 |
3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.477+3288G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487477 | |||||||
| chr20:56487508 | G | A | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
341 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.477+3319G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487508 | |||||||
| chr20:56487611 | T | C | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+3422T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487611 | |||||||
| chr20:56487691 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(34): Show |
48 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.477+3502C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487691 | |||||||
| chr20:56487729 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(4): Show |
10 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.477+3540G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487729 | |||||||
| chr20:56487815 | C | T | 20 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0035 others(17): Show |
37 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.477+3626C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487815 | |||||||
| chr20:56487897 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0069 |
3 | NA19003.hp2 NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.477+3708C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487897 | |||||||
| chr20:56487918 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+3729C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487918 | |||||||
| chr20:56488027 | G | A | 1 | a0001c0001t0008g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.477+3838G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488027 | |||||||
| chr20:56488099 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+3910G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488099 | |||||||
| chr20:56488190 | G | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(46): Show |
63 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.477+4001G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488190 | |||||||
| chr20:56488230 | G | A | 1 | a0002c0002t0002g0216 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.477+4041G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488230 | |||||||
| chr20:56488250 | A | G | 1 | a0002c0002t0001g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.477+4061A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488250 | |||||||
| chr20:56488290 | G | GGTGGAAG others(2626): Show |
1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+4145_477+4146i others(2635): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56488290 | ||||||
| chr20:56488484 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(134): Show |
186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.477+4295G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488484 | |||||||
| chr20:56488541 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.477+4352G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488541 | |||||||
| chr20:56488686 | C | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.477+4497C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488686 | |||||||
| chr20:56488705 | C | T | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.477+4516C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488705 | |||||||
| chr20:56488824 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+4635A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488824 | |||||||
| chr20:56488921 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(5): Show |
11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.477+4732C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488921 | |||||||
| chr20:56489063 | AT | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+4885delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56489063 | ||||||
| chr20:56489172 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(255): Show |
349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.477+4983T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489172 | |||||||
| chr20:56489221 | A | AT | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
250 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.477+5048dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56489221 | ||||||
| chr20:56489221 | A | ATT | 12 | a0001c0001t0001g0058 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG00438.hp1 HG02027.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+5047_477+5048d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56489221 | ||||||
| chr20:56489221 | A | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+5032A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489221 | |||||||
| chr20:56489221 | AT | A | 57 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(54): Show |
81 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.477+5048delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56489221 | ||||||
| chr20:56489253 | G | A | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+5064G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489253 | |||||||
| chr20:56489382 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA18945.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.477+5193C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489382 | |||||||
| chr20:56489411 | C | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(4): Show |
10 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.477+5222C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489411 | |||||||
| chr20:56489497 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+5308C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489497 | |||||||
| chr20:56489581 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0198 |
4 | HG01123.hp1 HG01934.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+5392C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489581 | |||||||
| chr20:56489604 | G | A | 1 | a0001c0007t0001g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.477+5415G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489604 | |||||||
| chr20:56489657 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.477+5468C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489657 | |||||||
| chr20:56489670 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(134): Show |
186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.477+5481C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489670 | |||||||
| chr20:56489779 | T | G | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
347 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.477+5590T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489779 | |||||||
| chr20:56489926 | G | C | 1 | a0002c0002t0001g0225 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.477+5737G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489926 | |||||||
| chr20:56489996 | A | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+5807A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489996 | |||||||
| chr20:56490121 | T | A | 1 | a0001c0001t0003g0071 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.477+5932T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490121 | |||||||
| chr20:56490157 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.477+5968A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490157 | |||||||
| chr20:56490165 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+5976C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490165 | |||||||
| chr20:56490255 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.477+6066C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490255 | |||||||
| chr20:56490316 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0198 |
4 | HG01123.hp1 HG01934.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+6127C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490316 | |||||||
| chr20:56490317 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.477+6128G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490317 | |||||||
| chr20:56490379 | C | A | 1 | a0001c0001t0002g0191 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.477+6190C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490379 | |||||||
| chr20:56490566 | G | T | 1 | a0001c0001t0001g0043 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.477+6377G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490566 | |||||||
| chr20:56490567 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.477+6378C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490567 | |||||||
| chr20:56490638 | C | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(45): Show |
62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.477+6449C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490638 | |||||||
| chr20:56490678 | G | T | 1 | a0002c0002t0001g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.477+6489G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490678 | |||||||
| chr20:56490757 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0173 |
5 | HG02145.hp1 HG02976.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+6568C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490757 | |||||||
| chr20:56490758 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.477+6569G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490758 | |||||||
| chr20:56491005 | G | A | 1 | a0001c0001t0002g0036 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.477+6816G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491005 | |||||||
| chr20:56491038 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0009g0130 |
2 | HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.477+6849T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491038 | |||||||
| chr20:56491157 | A | G | 1 | a0002c0002t0001g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.477+6968A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491157 | |||||||
| chr20:56491475 | C | T | 1 | a0002c0002t0001g0233 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.477+7286C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491475 | |||||||
| chr20:56491559 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+7370A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491559 | |||||||
| chr20:56491561 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+7372C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491561 | |||||||
| chr20:56491577 | T | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(35): Show |
49 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.477+7388T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491577 | |||||||
| chr20:56491667 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.477+7478A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491667 | |||||||
| chr20:56491830 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.477+7641A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491830 | |||||||
| chr20:56492056 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0072 |
3 | HG01070.hp1 HG01099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.477+7867G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492056 | |||||||
| chr20:56492079 | G | A | 106 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(103): Show |
144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.477+7890G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492079 | |||||||
| chr20:56492266 | C | T | 4 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0186 others(1): Show |
4 | HG01978.hp2 HG03942.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.477+8077C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492266 | |||||||
| chr20:56492355 | G | C | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+8166G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492355 | |||||||
| chr20:56492425 | G | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(108): Show |
152 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.477+8236G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492425 | |||||||
| chr20:56492461 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+8272T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492461 | |||||||
| chr20:56492463 | T | C | 3 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0217 |
3 | HG01175.hp2 HG01346.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.477+8274T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492463 | |||||||
| chr20:56492491 | G | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0042 a0001c0001t0002g0198 |
6 | HG00642.hp2 HG01123.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+8302G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492491 | |||||||
| chr20:56492577 | A | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+8388A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492577 | |||||||
| chr20:56492722 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+8533A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492722 | |||||||
| chr20:56492776 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.477+8587A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492776 | |||||||
| chr20:56492880 | TA | T | 111 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(108): Show |
152 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.477+8698delA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56492880 | ||||||
| chr20:56492949 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.477+8760G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492949 | |||||||
| chr20:56492982 | C | A | 2 | a0001c0001t0005g0113 a0001c0001t0005g0114 |
2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.477+8793C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492982 | |||||||
| chr20:56493091 | G | A | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+8902G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493091 | |||||||
| chr20:56493656 | C | CA | 5 | a0001c0001t0001g0043 a0001c0001t0001g0154 a0001c0001t0001g0219 others(2): Show |
6 | HG02559.hp1 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+9483dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56493656 | ||||||
| chr20:56493656 | C | CAA | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
147 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.477+9482_477+9483d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56493656 | ||||||
| chr20:56493656 | C | CAAA | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(79): Show |
105 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.477+9481_477+9483d others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56493656 | ||||||
| chr20:56493675 | C | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
376 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(373): Show |
intron_variant | MODIFIER | c.477+9486C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493675 | |||||||
| chr20:56493682 | T | C | 1 | a0001c0003t0002g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.477+9493T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493682 | |||||||
| chr20:56493893 | C | G | 6 | a0001c0001t0001g0127 a0001c0001t0002g0013 a0001c0001t0002g0036 others(3): Show |
9 | HG01255.hp1 HG02258.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.477+9704C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493893 | |||||||
| chr20:56493901 | T | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(271): Show |
370 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.477+9712T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493901 | |||||||
| chr20:56493910 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(77): Show |
103 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.477+9721G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493910 | |||||||
| chr20:56494060 | A | T | 1 | a0001c0001t0008g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.477+9871A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494060 | |||||||
| chr20:56494177 | T | A | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+9988T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494177 | |||||||
| chr20:56494211 | G | A | 1 | a0002c0002t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.477+10022G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494211 | |||||||
| chr20:56494235 | T | G | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
347 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.477+10046T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494235 | |||||||
| chr20:56494237 | A | T | 1 | a0001c0001t0001g0136 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.477+10048A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494237 | |||||||
| chr20:56494254 | T | C | 55 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(52): Show |
79 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.477+10065T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494254 | |||||||
| chr20:56494264 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.477+10075G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494264 | |||||||
| chr20:56494339 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
250 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.477+10150G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494339 | |||||||
| chr20:56494369 | T | C | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+10180T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494369 | |||||||
| chr20:56494373 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.477+10184A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494373 | |||||||
| chr20:56494410 | T | G | 1 | a0001c0001t0002g0037 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.477+10221T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494410 | |||||||
| chr20:56494438 | T | C | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+10249T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494438 | |||||||
| chr20:56494557 | T | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+10368T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494557 | |||||||
| chr20:56494828 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+10639C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494828 | |||||||
| chr20:56494932 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.477+10743A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494932 | |||||||
| chr20:56495020 | G | A | 58 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(55): Show |
82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.477+10831G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495020 | |||||||
| chr20:56495212 | A | T | 38 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(35): Show |
59 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.477+11023A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495212 | |||||||
| chr20:56495241 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.477+11052G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495241 | |||||||
| chr20:56495351 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.477+11162T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495351 | |||||||
| chr20:56495394 | G | A | 1 | a0001c0007t0001g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.477+11205G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495394 | |||||||
| chr20:56495483 | G | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(55): Show |
82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.477+11294G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495483 | |||||||
| chr20:56495608 | C | G | 53 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(50): Show |
76 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.477+11419C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495608 | |||||||
| chr20:56495609 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.477+11420A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495609 | |||||||
| chr20:56495687 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(136): Show |
188 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.477+11498A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495687 | |||||||
| chr20:56495742 | C | T | 107 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(104): Show |
145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.477+11553C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495742 | |||||||
| chr20:56495877 | A | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(45): Show |
62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.477+11688A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495877 | |||||||
| chr20:56495884 | A | C | 1 | a0001c0001t0002g0208 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.477+11695A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495884 | |||||||
| chr20:56495890 | C | G | 56 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(53): Show |
80 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.477+11701C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495890 | |||||||
| chr20:56496136 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(136): Show |
188 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.477+11947C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496136 | |||||||
| chr20:56496197 | A | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(55): Show |
82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.477+12008A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496197 | |||||||
| chr20:56496274 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.477+12085G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496274 | |||||||
| chr20:56496376 | T | G | 3 | a0001c0001t0001g0073 a0001c0001t0005g0113 a0001c0001t0005g0114 |
3 | HG01358.hp1 HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.477+12187T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496376 | |||||||
| chr20:56496379 | C | G | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+12190C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496379 | |||||||
| chr20:56496421 | G | A | 4 | a0002c0002t0001g0044 a0002c0002t0001g0224 a0002c0002t0001g0234 others(1): Show |
5 | HG02145.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+12232G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496421 | |||||||
| chr20:56496564 | T | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
249 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.477+12375T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496564 | |||||||
| chr20:56496583 | A | G | 54 | a0001c0001t0001g0150 a0001c0001t0002g0001 a0001c0001t0002g0009 others(51): Show |
77 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.477+12394A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496583 | |||||||
| chr20:56496617 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+12428C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496617 | |||||||
| chr20:56496626 | G | A | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+12437G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496626 | |||||||
| chr20:56496711 | C | A | 1 | a0001c0001t0002g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.477+12522C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496711 | |||||||
| chr20:56496804 | G | A | 1 | a0001c0001t0008g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.477+12615G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496804 | |||||||
| chr20:56497160 | T | C | 1 | a0001c0001t0008g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.477+12971T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497160 | |||||||
| chr20:56497231 | C | T | 1 | a0001c0007t0001g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.477+13042C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497231 | |||||||
| chr20:56497238 | A | G | 2 | a0001c0001t0001g0027 a0001c0006t0001g0095 |
3 | HG02683.hp1 HG03490.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.477+13049A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497238 | |||||||
| chr20:56497416 | A | G | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
341 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.477+13227A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497416 | |||||||
| chr20:56497427 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(5): Show |
11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.477+13238C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497427 | |||||||
| chr20:56497452 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.477+13263A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497452 | |||||||
| chr20:56497519 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.477+13330A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497519 | |||||||
| chr20:56497754 | A | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+13565A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497754 | |||||||
| chr20:56497909 | A | G | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.477+13720A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497909 | |||||||
| chr20:56497937 | G | A | 1 | a0002c0002t0001g0047 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.477+13748G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497937 | |||||||
| chr20:56498107 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.477+13918T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498107 | |||||||
| chr20:56498108 | A | AT | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
341 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.477+13921dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56498108 | ||||||
| chr20:56498171 | T | C | 1 | a0001c0001t0006g0074 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.477+13982T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498171 | |||||||
| chr20:56498330 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(34): Show |
48 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.477+14141G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498330 | |||||||
| chr20:56498590 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.477+14401A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498590 | |||||||
| chr20:56498667 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.477+14478T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498667 | |||||||
| chr20:56498752 | T | C | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+14563T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498752 | |||||||
| chr20:56498771 | T | A | 41 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(38): Show |
62 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.478-14544T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498771 | |||||||
| chr20:56499194 | C | CT | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0058 others(15): Show |
22 | HG00280.hp2 HG01978.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.478-14101dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56499194 | ||||||
| chr20:56499194 | CT | C | 20 | a0001c0001t0001g0075 a0001c0001t0001g0121 a0001c0001t0001g0133 others(17): Show |
20 | HG00323.hp2 HG00558.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.478-14101delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56499194 | ||||||
| chr20:56499282 | C | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
84 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.478-14033C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499282 | |||||||
| chr20:56499337 | T | C | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-13978T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499337 | |||||||
| chr20:56499389 | G | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.478-13926G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499389 | |||||||
| chr20:56499414 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-13901C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499414 | |||||||
| chr20:56499567 | T | A | 4 | a0001c0003t0002g0252 a0001c0003t0002g0253 a0001c0003t0002g0254 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-13748T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499567 | |||||||
| chr20:56499752 | T | C | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-13563T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499752 | |||||||
| chr20:56499806 | A | T | 1 | a0001c0001t0001g0033 | 2 | HG00642.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.478-13509A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499806 | |||||||
| chr20:56499840 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.478-13475G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499840 | |||||||
| chr20:56500033 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-13282C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500033 | |||||||
| chr20:56500194 | A | G | 56 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(53): Show |
80 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.478-13121A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500194 | |||||||
| chr20:56500289 | G | C | 1 | a0002c0002t0001g0247 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.478-13026G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500289 | |||||||
| chr20:56500309 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.478-13006C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500309 | |||||||
| chr20:56500333 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-12982C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500333 | |||||||
| chr20:56500532 | C | A | 1 | a0001c0001t0001g0273 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.478-12783C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500532 | |||||||
| chr20:56500582 | A | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(5): Show |
11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.478-12733A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500582 | |||||||
| chr20:56500827 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478-12488G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500827 | |||||||
| chr20:56500827 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.478-12488G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500827 | |||||||
| chr20:56500935 | G | A | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.478-12380G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500935 | |||||||
| chr20:56500978 | T | A | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-12337T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500978 | |||||||
| chr20:56500979 | T | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
342 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.478-12336T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500979 | |||||||
| chr20:56501005 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(45): Show |
62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.478-12310C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501005 | |||||||
| chr20:56501087 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0155 a0001c0001t0001g0183 |
3 | HG02559.hp2 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.478-12228A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501087 | |||||||
| chr20:56501091 | C | G | 1 | a0001c0001t0001g0282 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.478-12224C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501091 | |||||||
| chr20:56501155 | A | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-12160A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501155 | |||||||
| chr20:56501203 | CT | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(75): Show |
102 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.478-12101delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56501203 | ||||||
| chr20:56501605 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-11710A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501605 | |||||||
| chr20:56501829 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0270 a0001c0001t0001g0276 |
4 | HG02015.hp1 NA18951.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-11486A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501829 | |||||||
| chr20:56502091 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(136): Show |
188 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.478-11224A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502091 | |||||||
| chr20:56502277 | A | T | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-11038A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502277 | |||||||
| chr20:56502284 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.478-11031T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502284 | |||||||
| chr20:56502475 | G | A | 1 | a0001c0001t0008g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.478-10840G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502475 | |||||||
| chr20:56502543 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.478-10772G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502543 | |||||||
| chr20:56502656 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.478-10659G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502656 | |||||||
| chr20:56502861 | C | T | 52 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(49): Show |
75 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.478-10454C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502861 | |||||||
| chr20:56502897 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.478-10418G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502897 | |||||||
| chr20:56502911 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(134): Show |
186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.478-10404G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502911 | |||||||
| chr20:56503042 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.478-10273C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503042 | |||||||
| chr20:56503434 | C | T | 1 | a0002c0002t0001g0248 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.478-9881C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503434 | |||||||
| chr20:56503469 | ACAAATGG others(3): Show |
A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.478-9843_478-9834d others(12): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56503469 | ||||||
| chr20:56503477 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
185 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.478-9838T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503477 | |||||||
| chr20:56503513 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0070 a0001c0001t0001g0092 others(3): Show |
8 | NA18950.hp2 NA18955.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.478-9802C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503513 | |||||||
| chr20:56503517 | G | A | 57 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(54): Show |
81 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.478-9798G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503517 | |||||||
| chr20:56503660 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.478-9655T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503660 | |||||||
| chr20:56503733 | T | A | 57 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(54): Show |
81 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.478-9582T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503733 | |||||||
| chr20:56503963 | GACAC | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0173 |
5 | HG02145.hp1 HG02976.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-9341_478-9338d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56503963 | ||||||
| chr20:56503980 | A | G | 57 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(54): Show |
81 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.478-9335A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503980 | |||||||
| chr20:56503991 | C | G | 1 | a0001c0007t0001g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.478-9324C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503991 | |||||||
| chr20:56504135 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.478-9180T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504135 | |||||||
| chr20:56504216 | A | T | 1 | a0001c0001t0002g0195 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.478-9099A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504216 | |||||||
| chr20:56504324 | G | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(52): Show |
79 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.478-8991G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504324 | |||||||
| chr20:56504337 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.478-8978G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504337 | |||||||
| chr20:56504343 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.478-8972C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504343 | |||||||
| chr20:56504566 | G | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
345 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.478-8749G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504566 | |||||||
| chr20:56504582 | A | T | 1 | a0001c0001t0002g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.478-8733A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504582 | |||||||
| chr20:56504766 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.478-8549G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504766 | |||||||
| chr20:56504780 | T | G | 1 | a0001c0001t0002g0198 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.478-8535T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504780 | |||||||
| chr20:56504902 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
254 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.478-8413T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504902 | |||||||
| chr20:56504996 | T | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
344 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.478-8319T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504996 | |||||||
| chr20:56505165 | C | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-8150C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505165 | |||||||
| chr20:56505217 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.478-8098T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505217 | |||||||
| chr20:56505267 | G | A | 1 | a0002c0002t0001g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.478-8048G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505267 | |||||||
| chr20:56505358 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.478-7957C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505358 | |||||||
| chr20:56505407 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.478-7908G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505407 | |||||||
| chr20:56505487 | C | CATA | 6 | a0001c0001t0001g0090 a0001c0001t0002g0251 a0001c0007t0001g0053 others(3): Show |
6 | HG00738.hp1 HG02040.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-7800_478-7798d others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | ||||||
| chr20:56505487 | C | CATAATA | 13 | a0001c0001t0001g0033 a0001c0001t0001g0073 a0001c0001t0001g0164 others(10): Show |
14 | HG00642.hp1 HG00733.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.478-7803_478-7798d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | ||||||
| chr20:56505487 | C | CATAATAA others(2): Show |
102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.478-7806_478-7798d others(11): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | ||||||
| chr20:56505487 | C | CATAATAA others(5): Show |
98 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
127 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.478-7809_478-7798d others(14): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | ||||||
| chr20:56505487 | C | CATAATAA others(8): Show |
22 | a0001c0001t0001g0031 a0001c0001t0001g0049 a0001c0001t0001g0063 others(19): Show |
25 | HG00558.hp2 HG00639.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.478-7812_478-7798d others(17): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | ||||||
| chr20:56505487 | C | CATAATAA others(11): Show |
8 | a0001c0001t0001g0260 a0001c0001t0001g0265 a0001c0001t0001g0266 others(5): Show |
10 | HG01074.hp1 HG01167.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.478-7815_478-7798d others(20): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | ||||||
| chr20:56505487 | C | CATAATAA others(14): Show |
3 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0004g0078 |
3 | HG00673.hp2 HG01952.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.478-7818_478-7798d others(23): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | ||||||
| chr20:56505487 | CATA | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0071 |
4 | HG00609.hp2 NA18952.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-7800_478-7798d others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | ||||||
| chr20:56505502 | A | AATAATAA others(4): Show |
1 | a0001c0001t0003g0091 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.478-7811_478-7801d others(13): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505502 | ||||||
| chr20:56505517 | A | AATAATAA others(7): Show |
1 | a0001c0001t0001g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.478-7798_478-7797i others(16): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505517 | |||||||
| chr20:56505518 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.478-7797T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505518 | |||||||
| chr20:56505546 | C | T | 1 | a0002c0002t0001g0240 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.478-7769C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505546 | |||||||
| chr20:56505547 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-7768G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505547 | |||||||
| chr20:56505549 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.478-7766C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505549 | |||||||
| chr20:56505709 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.478-7606G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505709 | |||||||
| chr20:56505764 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.478-7551C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505764 | |||||||
| chr20:56505809 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.478-7506A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505809 | |||||||
| chr20:56505816 | C | T | 1 | a0002c0008t0001g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.478-7499C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505816 | |||||||
| chr20:56505874 | A | G | 1 | a0001c0001t0002g0218 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.478-7441A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505874 | |||||||
| chr20:56505884 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-7431G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505884 | |||||||
| chr20:56505969 | T | C | 1 | a0001c0001t0008g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.478-7346T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505969 | |||||||
| chr20:56506106 | A | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
345 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.478-7209A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506106 | |||||||
| chr20:56506200 | G | A | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.478-7115G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506200 | |||||||
| chr20:56506297 | C | T | 54 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(51): Show |
78 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.478-7018C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506297 | |||||||
| chr20:56506323 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
251 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.478-6992A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506323 | |||||||
| chr20:56506328 | A | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(34): Show |
48 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.478-6987A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506328 | |||||||
| chr20:56506351 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.478-6964G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506351 | |||||||
| chr20:56506433 | T | TG | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
347 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.478-6881dupG | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56506433 | ||||||
| chr20:56506490 | A | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0218 |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-6825A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506490 | |||||||
| chr20:56506562 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.478-6753A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506562 | |||||||
| chr20:56506763 | C | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(33): Show |
47 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.478-6552C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506763 | |||||||
| chr20:56506796 | C | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0219 a0001c0001t0010g0166 |
4 | HG01175.hp1 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-6519C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506796 | |||||||
| chr20:56506873 | T | A | 20 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0035 others(17): Show |
37 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.478-6442T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506873 | |||||||
| chr20:56506891 | G | C | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-6424G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506891 | |||||||
| chr20:56506995 | T | C | 55 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(52): Show |
79 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.478-6320T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506995 | |||||||
| chr20:56507008 | A | AT | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-6300dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56507008 | ||||||
| chr20:56507100 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-6215A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507100 | |||||||
| chr20:56507137 | A | G | 1 | a0002c0002t0001g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.478-6178A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507137 | |||||||
| chr20:56507146 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.478-6169T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507146 | |||||||
| chr20:56507152 | A | AT | 3 | a0001c0001t0001g0223 a0001c0001t0002g0221 a0001c0001t0002g0222 |
3 | HG02976.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.478-6159dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56507152 | ||||||
| chr20:56507269 | T | C | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-6046T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507269 | |||||||
| chr20:56507335 | C | T | 1 | a0002c0002t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.478-5980C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507335 | |||||||
| chr20:56507361 | G | A | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-5954G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507361 | |||||||
| chr20:56507399 | G | C | 1 | a0001c0001t0002g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.478-5916G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507399 | |||||||
| chr20:56507692 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.478-5623A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507692 | |||||||
| chr20:56507753 | C | T | 2 | a0001c0001t0002g0189 a0001c0001t0002g0211 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.478-5562C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507753 | |||||||
| chr20:56507760 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.478-5555A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507760 | |||||||
| chr20:56507933 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.478-5382C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507933 | |||||||
| chr20:56508282 | T | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-5033T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508282 | |||||||
| chr20:56508295 | G | GA | 38 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0049 others(35): Show |
49 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.478-5011dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56508295 | ||||||
| chr20:56508357 | G | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0219 |
3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.478-4958G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508357 | |||||||
| chr20:56508375 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.478-4940A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508375 | |||||||
| chr20:56508422 | G | T | 112 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(109): Show |
153 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.478-4893G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508422 | |||||||
| chr20:56508633 | C | T | 1 | a0001c0001t0001g0005 | 6 | NA18963.hp2 NA18970.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.478-4682C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508633 | |||||||
| chr20:56508723 | T | C | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-4592T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508723 | |||||||
| chr20:56508760 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.478-4555A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508760 | |||||||
| chr20:56508937 | A | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(47): Show |
64 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.478-4378A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508937 | |||||||
| chr20:56509176 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
337 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.478-4139A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509176 | |||||||
| chr20:56509239 | T | A | 11 | a0001c0001t0002g0014 a0001c0001t0002g0038 a0001c0001t0002g0190 others(8): Show |
12 | HG00735.hp2 HG01106.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.478-4076T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509239 | |||||||
| chr20:56509299 | A | G | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-4016A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509299 | |||||||
| chr20:56509449 | C | G | 1 | a0001c0001t0002g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.478-3866C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509449 | |||||||
| chr20:56509577 | G | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-3738G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509577 | |||||||
| chr20:56509611 | C | CA | 68 | a0001c0001t0001g0093 a0001c0001t0001g0174 a0001c0001t0002g0001 others(65): Show |
96 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.478-3688dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56509611 | ||||||
| chr20:56509859 | T | A | 1 | a0001c0001t0002g0037 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.478-3456T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509859 | |||||||
| chr20:56509988 | CA | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0033 others(32): Show |
48 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.478-3315delA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56509988 | ||||||
| chr20:56510006 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(79): Show |
105 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.478-3309A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510006 | |||||||
| chr20:56510016 | A | G | 1 | a0001c0001t0007g0118 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.478-3299A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510016 | |||||||
| chr20:56510110 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
344 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.478-3205T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510110 | |||||||
| chr20:56510196 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.478-3119T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510196 | |||||||
| chr20:56510231 | G | A | 4 | a0002c0002t0001g0044 a0002c0002t0001g0224 a0002c0002t0001g0234 others(1): Show |
5 | HG02145.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-3084G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510231 | |||||||
| chr20:56510331 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.478-2984C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510331 | |||||||
| chr20:56510410 | A | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-2905A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510410 | |||||||
| chr20:56510428 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
5 | HG00733.hp1 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-2887C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510428 | |||||||
| chr20:56510429 | A | G | 1 | a0002c0002t0001g0240 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.478-2886A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510429 | |||||||
| chr20:56510640 | A | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-2675A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510640 | |||||||
| chr20:56510710 | C | T | 1 | a0001c0001t0002g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.478-2605C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510710 | |||||||
| chr20:56510716 | G | A | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-2599G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510716 | |||||||
| chr20:56510719 | T | A | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.478-2596T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510719 | |||||||
| chr20:56510918 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.478-2397A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510918 | |||||||
| chr20:56510986 | TC | T | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-2327delC | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56510986 | ||||||
| chr20:56511007 | T | C | 37 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(34): Show |
58 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.478-2308T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511007 | |||||||
| chr20:56511102 | G | A | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.478-2213G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511102 | |||||||
| chr20:56511120 | A | T | 2 | a0001c0001t0001g0223 a0001c0001t0010g0166 |
2 | HG01175.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.478-2195A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511120 | |||||||
| chr20:56511220 | C | G | 1 | a0002c0002t0001g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.478-2095C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511220 | |||||||
| chr20:56511225 | G | T | 52 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(49): Show |
75 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.478-2090G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511225 | |||||||
| chr20:56511338 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.478-1977G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511338 | |||||||
| chr20:56511385 | G | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | NA18942.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.478-1930G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511385 | |||||||
| chr20:56511390 | G | T | 1 | a0002c0002t0001g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.478-1925G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511390 | |||||||
| chr20:56511432 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0223 |
2 | HG02129.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.478-1883A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511432 | |||||||
| chr20:56511440 | A | ATTG | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(47): Show |
64 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.478-1873_478-1871d others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56511440 | ||||||
| chr20:56511448 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.478-1867C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511448 | |||||||
| chr20:56511545 | C | A | 1 | a0001c0001t0002g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-1770C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511545 | |||||||
| chr20:56511643 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1672G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511643 | |||||||
| chr20:56511677 | C | G | 1 | a0001c0001t0001g0266 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.478-1638C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511677 | |||||||
| chr20:56511840 | CT | C | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1465delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56511840 | ||||||
| chr20:56511856 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | NA18942.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.478-1459G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511856 | |||||||
| chr20:56511896 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.478-1419G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511896 | |||||||
| chr20:56511926 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.478-1389G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511926 | |||||||
| chr20:56511985 | A | C | 41 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(38): Show |
62 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.478-1330A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511985 | |||||||
| chr20:56511992 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1323C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511992 | |||||||
| chr20:56512259 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0081 |
3 | NA18945.hp1 NA18951.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.478-1056G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512259 | |||||||
| chr20:56512487 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-828A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512487 | |||||||
| chr20:56512494 | GCTCA | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0219 |
3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.478-814_478-811del others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56512494 | ||||||
| chr20:56512547 | G | T | 1 | a0001c0001t0001g0018 | 3 | NA18944.hp1 NA18967.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.478-768G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512547 | |||||||
| chr20:56512559 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.478-756C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512559 | |||||||
| chr20:56512575 | A | T | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0277 |
3 | NA18974.hp1 NA18992.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.478-740A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512575 | |||||||
| chr20:56512602 | T | C | 1 | a0001c0001t0002g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.478-713T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512602 | |||||||
| chr20:56512608 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0059 a0001c0001t0001g0069 others(1): Show |
5 | HG03139.hp2 NA18964.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-707C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512608 | |||||||
| chr20:56512712 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-603C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512712 | |||||||
| chr20:56512754 | T | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-561T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512754 | |||||||
| chr20:56512803 | C | G | 1 | a0001c0001t0008g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.478-512C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512803 | |||||||
| chr20:56512845 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-470C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512845 | |||||||
| chr20:56512908 | T | C | 57 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(54): Show |
81 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.478-407T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512908 | |||||||
| chr20:56512941 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.478-374C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512941 | |||||||
| chr20:56513138 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-177C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56513138 | |||||||
| chr20:56513220 | G | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(5): Show |
11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.478-95G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56513220 | |||||||
| chr20:56513450 | CGCCCA | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(4): Show |
10 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.591+27_591+31delAG others(3): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56513450 | ||||||
| chr20:56513484 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.591+56C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56513484 | |||||||
| chr20:56513635 | G | A | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+207G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56513635 | |||||||
| chr20:56513742 | T | C | 54 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0014 others(51): Show |
77 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.591+314T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56513742 | |||||||
| chr20:56513951 | A | AGGCCTGG others(3): Show |
8 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(5): Show |
11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.591+534_591+543dup others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56513951 | ||||||
| chr20:56513975 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(76): Show |
102 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.591+547G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56513975 | |||||||
| chr20:56514036 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.591+608C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514036 | |||||||
| chr20:56514150 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.591+722G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514150 | |||||||
| chr20:56514160 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.591+732G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514160 | |||||||
| chr20:56514205 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.591+777C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514205 | |||||||
| chr20:56514250 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.591+822A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514250 | |||||||
| chr20:56514350 | TA | T | 8 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0098 others(5): Show |
8 | HG02027.hp1 HG02897.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.591+935delA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56514350 | ||||||
| chr20:56514681 | A | G | 2 | a0001c0001t0002g0197 a0001c0001t0010g0166 |
2 | HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.591+1253A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514681 | |||||||
| chr20:56514884 | T | C | 1 | a0001c0001t0002g0210 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.591+1456T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514884 | |||||||
| chr20:56514903 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0087 |
3 | HG02523.hp2 NA19003.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.591+1475C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514903 | |||||||
| chr20:56514996 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0219 |
3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.591+1568G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514996 | |||||||
| chr20:56515035 | T | TA | 8 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0069 others(5): Show |
8 | HG00733.hp1 HG01175.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+1622dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515035 | ||||||
| chr20:56515338 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.592-1597G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515338 | |||||||
| chr20:56515559 | G | A | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-1376G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515559 | |||||||
| chr20:56515575 | C | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.592-1360C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515575 | |||||||
| chr20:56515575 | CAG | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(37): Show |
52 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.592-1336_592-1335d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515575 | ||||||
| chr20:56515575 | CAGAG | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0264 a0001c0001t0001g0268 others(7): Show |
12 | HG01256.hp2 HG02809.hp2 HG03041.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-1338_592-1335d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515575 | ||||||
| chr20:56515575 | CAGAGAG | C | 6 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0037 others(3): Show |
11 | HG01109.hp2 HG01123.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.592-1340_592-1335d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515575 | ||||||
| chr20:56515591 | GAGAGAGA others(9): Show |
G | 1 | a0001c0001t0001g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.592-1342_592-1327d others(18): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515591 | ||||||
| chr20:56515593 | GAGAGAGA others(1): Show |
G | 15 | a0001c0001t0001g0223 a0001c0001t0002g0001 a0001c0001t0002g0038 others(12): Show |
16 | HG00642.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.592-1340_592-1333d others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515593 | ||||||
| chr20:56515593 | GAGAGAGA others(3): Show |
G | 21 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0035 others(18): Show |
34 | HG00280.hp1 HG00544.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.592-1340_592-1331d others(12): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515593 | ||||||
| chr20:56515593 | GAGAGAGA others(7): Show |
G | 6 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0040 others(3): Show |
9 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-1340_592-1327d others(16): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515593 | ||||||
| chr20:56515593 | GAGAGAGA others(9): Show |
G | 1 | a0001c0001t0002g0001 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.592-1340_592-1325d others(18): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515593 | ||||||
| chr20:56515595 | G | C | 5 | a0001c0001t0002g0197 a0001c0001t0002g0209 a0001c0001t0002g0213 others(2): Show |
5 | HG01106.hp2 HG01496.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-1340G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515595 | |||||||
| chr20:56515595 | G | GAC | 3 | a0001c0001t0001g0267 a0001c0001t0001g0278 a0001c0001t0001g0281 |
3 | HG01975.hp2 NA18962.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.592-1339_592-1338i others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | ||||||
| chr20:56515595 | GAGAGAC | G | 4 | a0001c0001t0001g0258 a0001c0001t0001g0271 a0001c0001t0001g0280 others(1): Show |
4 | HG00597.hp1 HG02027.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-1338_592-1333d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | ||||||
| chr20:56515595 | GAGAGACA others(3): Show |
G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0205 |
2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.592-1338_592-1329d others(12): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | ||||||
| chr20:56515595 | GAGAGACA others(5): Show |
G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
9 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.592-1338_592-1327d others(14): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | ||||||
| chr20:56515595 | GAGAGACA others(7): Show |
G | 1 | a0001c0001t0001g0260 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.592-1338_592-1325d others(16): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | ||||||
| chr20:56515595 | GAGAGACA others(11): Show |
G | 8 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0079 others(5): Show |
8 | HG00558.hp1 HG02056.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.592-1338_592-1321d others(20): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | ||||||
| chr20:56515595 | GAGAGACA others(13): Show |
G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
174 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.592-1338_592-1319d others(22): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | ||||||
| chr20:56515595 | GAGAGACA others(15): Show |
G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.592-1338_592-1317d others(24): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | ||||||
| chr20:56515595 | GAGAGACA others(17): Show |
G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0126 |
2 | HG02300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.592-1338_592-1315d others(26): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | ||||||
| chr20:56515597 | G | C | 19 | a0001c0001t0001g0256 a0001c0001t0001g0262 a0001c0001t0001g0267 others(16): Show |
20 | HG00673.hp2 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.592-1338G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515597 | |||||||
| chr20:56515597 | GAGAC | G | 13 | a0002c0002t0001g0044 a0002c0002t0001g0045 a0002c0002t0001g0048 others(10): Show |
14 | HG00323.hp2 HG01070.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.592-1336_592-1333d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | ||||||
| chr20:56515597 | GAGACAC | G | 4 | a0001c0001t0002g0251 a0002c0002t0001g0235 a0002c0002t0001g0241 others(1): Show |
4 | HG01928.hp2 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-1336_592-1331d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | ||||||
| chr20:56515597 | GAGACACA others(5): Show |
G | 1 | a0001c0001t0008g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.592-1336_592-1325d others(14): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | ||||||
| chr20:56515597 | GAGACACA others(9): Show |
G | 1 | a0001c0007t0001g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.592-1336_592-1321d others(18): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | ||||||
| chr20:56515597 | GAGACACA others(13): Show |
G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0109 a0001c0001t0001g0125 |
3 | HG01891.hp1 HG03831.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.592-1336_592-1317d others(22): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | ||||||
| chr20:56515599 | G | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(42): Show |
55 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.592-1336G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515599 | |||||||
| chr20:56515599 | GAC | G | 3 | a0002c0002t0001g0044 a0002c0002t0001g0047 a0002c0002t0002g0216 |
3 | HG00639.hp1 HG01168.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.592-1294_592-1293d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515599 | ||||||
| chr20:56515599 | GACAC | G | 2 | a0002c0002t0001g0046 a0002c0002t0001g0047 |
3 | HG01074.hp2 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.592-1296_592-1293d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515599 | ||||||
| chr20:56515601 | C | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.592-1334C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515601 | |||||||
| chr20:56515603 | C | G | 2 | a0001c0001t0010g0166 a0002c0002t0001g0047 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.592-1332C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515603 | |||||||
| chr20:56515605 | C | G | 2 | a0001c0001t0010g0166 a0002c0002t0001g0047 |
3 | HG00639.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.592-1330C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515605 | |||||||
| chr20:56515607 | C | G | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.592-1328C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515607 | |||||||
| chr20:56515665 | G | C | 2 | a0001c0001t0001g0287 a0001c0001t0002g0179 |
2 | HG02155.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.592-1270G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515665 | |||||||
| chr20:56515665 | G | GAC | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.592-1243_592-1242d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | ||||||
| chr20:56515665 | G | GACAC | 11 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0056 others(8): Show |
13 | HG01123.hp2 HG01167.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.592-1245_592-1242d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | ||||||
| chr20:56515665 | G | GACACAC | 55 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(52): Show |
74 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.592-1247_592-1242d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | ||||||
| chr20:56515665 | G | GACACACA others(1): Show |
8 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0061 others(5): Show |
10 | HG01168.hp2 HG02683.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-1249_592-1242d others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | ||||||
| chr20:56515665 | G | GACACACA others(3): Show |
18 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0064 others(15): Show |
20 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(17): Show |
intron_variant | MODIFIER | c.592-1251_592-1242d others(12): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | ||||||
| chr20:56515665 | GAC | G | 10 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(7): Show |
10 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.592-1243_592-1242d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | ||||||
| chr20:56515665 | GACACACA others(1): Show |
G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0173 a0001c0001t0001g0269 |
6 | HG02145.hp1 HG02976.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-1249_592-1242d others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | ||||||
| chr20:56515693 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.592-1242C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515693 | |||||||
| chr20:56515842 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0270 |
3 | NA18951.hp2 NA18953.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.592-1093C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515842 | |||||||
| chr20:56515912 | G | T | 1 | a0002c0002t0001g0238 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.592-1023G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515912 | |||||||
| chr20:56516150 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.592-785G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56516150 | |||||||
| chr20:56516214 | AC | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0167 others(4): Show |
10 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.592-719delC | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56516214 | ||||||
| chr20:56516326 | GTTTGT | G | 5 | a0001c0001t0002g0251 a0001c0003t0002g0252 a0001c0003t0002g0253 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-605_592-601del others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56516326 | ||||||
| chr20:56516713 | A | T | 1 | a0002c0002t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.592-222A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56516713 | |||||||
| chr20:56516853 | A | C | 1 | a0001c0001t0010g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.592-82A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56516853 | |||||||
| chr20:56517007 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.646+18A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 7/8 | chr20 | 56517007 | |||||||
| chr20:56517315 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+114T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517315 | |||||||
| chr20:56517329 | G | A | 1 | a0001c0001t0002g0040 | 2 | NA18986.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.742+128G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517329 | |||||||
| chr20:56517350 | G | T | 1 | a0002c0002t0001g0046 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.742+149G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517350 | |||||||
| chr20:56517446 | A | T | 1 | a0001c0001t0002g0037 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.742+245A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517446 | |||||||
| chr20:56517536 | C | T | 1 | a0002c0002t0001g0230 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.742+335C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517536 | |||||||
| chr20:56517585 | G | A | 7 | a0001c0001t0002g0189 a0001c0001t0002g0191 a0001c0001t0002g0192 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.742+384G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517585 | |||||||
| chr20:56517590 | G | A | 3 | a0001c0001t0002g0037 a0001c0001t0002g0179 a0001c0001t0002g0180 |
4 | HG01261.hp1 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+389G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517590 | |||||||
| chr20:56517770 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.743-317G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517770 | |||||||
| chr20:56517864 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG00642.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.743-223G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517864 | |||||||
| chr20:56517955 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0176 others(2): Show |
8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.743-132G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517955 |