Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84154 |
| ensemblid | ENSG00000197498.13 |
| hgncid | 20870 |
| symbol | RPF2 |
| name | ribosome production factor 2 homolog |
| refseq_nuc | NM_032194.3 |
| refseq_prot | NP_115570.1 |
| ensembl_nuc | ENST00000441448.7 |
| ensembl_prot | ENSP00000402338.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 110982038 |
| end | 111028263 |
| strand | + |
| ver | v1.2 |
| region | chr6:110982038-111028263 |
| region5000 | chr6:110977038-111033263 |
| regionname0 | RPF2_chr6_110982038_111028263 |
| regionname5000 | RPF2_chr6_110977038_111033263 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 306 | 345 | 63 | 65 | 159 | 10 | 46 | 122 | RPF2_chr6_110977038_111033263 | RPF2 | MDTLD others(301): Show |
chr6 | 110977038 | 111033263 |
| a0002 | 0/0 | 306 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | MDTLD others(301): Show |
chr6 | 110977038 | 111033263 |
| a0003 | 0/0 | 306 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | MDTLD others(301): Show |
chr6 | 110977038 | 111033263 |
| a0004 | 0/0 | 306 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | MDTLD others(301): Show |
chr6 | 110977038 | 111033263 |
| a0005 | 0/0 | 306 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | MDTLD others(301): Show |
chr6 | 110977038 | 111033263 |
| a0006 | 0/0 | 306 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | MDTLD others(301): Show |
chr6 | 110977038 | 111033263 |
| a0007 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | MDTLD others(298): Show |
chr6 | 110977038 | 111033263 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 918 | 343 | 61 | 65 | 159 | 10 | 46 | RPF2_chr6_110977038_111033263 | RPF2 | ATGGA others(913): Show |
chr6 | 110977038 | 111033263 | ||
| a0001c0005 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | ATGGA others(913): Show |
chr6 | 110977038 | 111033263 | ||
| a0001c0006 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | ATGGA others(913): Show |
chr6 | 110977038 | 111033263 | ||
| a0002c0002 | 0/0 | 918 | 6 | 5 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | ATGGA others(913): Show |
chr6 | 110977038 | 111033263 | ||
| a0003c0003 | 0/0 | 918 | 4 | 4 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | ATGGA others(913): Show |
chr6 | 110977038 | 111033263 | ||
| a0004c0004 | 0/0 | 918 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | ATGGA others(913): Show |
chr6 | 110977038 | 111033263 | ||
| a0005c0009 | 0/0 | 918 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | ATGGA others(913): Show |
chr6 | 110977038 | 111033263 | ||
| a0006c0008 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | ATGGA others(913): Show |
chr6 | 110977038 | 111033263 | ||
| a0007c0007 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | ATGGA others(913): Show |
chr6 | 110977038 | 111033263 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3671 | 118 | 5 | 26 | 66 | 3 | 18 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0002 | 0/0 | 3671 | 82 | 12 | 9 | 46 | 3 | 12 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0003 | 0/0 | 3676 | 55 | 14 | 8 | 25 | 0 | 8 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0004 | 1/1 | 3671 | 38 | 11 | 15 | 1 | 4 | 5 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0005 | 0/0 | 3671 | 10 | 0 | 0 | 10 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0006 | 0/0 | 3677 | 8 | 1 | 3 | 2 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3672): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0007 | 0/0 | 3676 | 6 | 6 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0008 | 0/0 | 3671 | 5 | 5 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0011 | 0/0 | 3671 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0012 | 0/0 | 3671 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0013 | 0/0 | 3676 | 2 | 1 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0014 | 0/0 | 3676 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0015 | 0/0 | 3671 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0016 | 0/0 | 3671 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0017 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0019 | 0/0 | 3671 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0020 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3667): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0021 | 0/0 | 3677 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3672): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0022 | 0/0 | 3677 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3672): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0023 | 0/0 | 3677 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3672): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0024 | 0/0 | 3671 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0025 | 0/0 | 3676 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0026 | 0/0 | 3676 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0001c0001t0028 | 0/0 | 3671 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0001c0005t0027 | 0/0 | 3676 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0001c0006t0004 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0002c0002t0009 | 0/0 | 3671 | 3 | 3 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0002c0002t0010 | 0/0 | 3676 | 3 | 2 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0003c0003t0003 | 0/0 | 3676 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0003c0003t0004 | 0/0 | 3671 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0004c0004t0002 | 0/0 | 3671 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0005c0009t0001 | 0/0 | 3671 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| a0006c0008t0007 | 0/0 | 3676 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3671): Show |
chr6 | 110977038 | 111033263 |
| a0007c0007t0018 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | GTTCC others(3666): Show |
chr6 | 110977038 | 111033263 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0001 | 1/0 | 6 | 0 | 4 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0005g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0006g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0012g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0012g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0013g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0014g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0014g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0015g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0016g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0017g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0019g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0020g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0021g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0022g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0023g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0024g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0025g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0026g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0001t0028g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0005t0027g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0001c0006t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0002c0002t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0002c0002t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0002c0002t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0002c0002t0010g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0002c0002t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0002c0002t0010g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0003c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0003c0003t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0003c0003t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0003c0003t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0004c0004t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0004c0004t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0005c0009t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0006c0008t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| a0007c0007t0018g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | GBR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | GBR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | FIN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0096 | EUR | FIN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0114 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00741 | hp1 | a0001 | c0001 | t0013 | g0186 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0090 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01109 | hp1 | a0001 | c0001 | t0025 | g0167 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01346 | hp1 | a0001 | c0001 | t0016 | g0041 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01433 | hp2 | a0002 | c0002 | t0010 | g0259 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0079 | EUR | IBS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0097 | EUR | IBS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01884 | hp1 | a0003 | c0003 | t0004 | g0033 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01884 | hp2 | a0001 | c0001 | t0015 | g0188 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01952 | hp1 | a0001 | c0001 | t0022 | g0123 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02040 | hp2 | a0005 | c0009 | t0001 | g0077 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02055 | hp1 | a0004 | c0004 | t0002 | g0242 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02083 | hp2 | a0001 | c0001 | t0026 | g0155 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02135 | hp2 | a0001 | c0001 | t0014 | g0192 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02258 | hp1 | a0003 | c0003 | t0003 | g0032 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02258 | hp2 | a0001 | c0006 | t0004 | g0027 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0325 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0152 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02572 | hp1 | a0003 | c0003 | t0003 | g0185 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0217 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02647 | hp2 | a0002 | c0002 | t0009 | g0261 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02683 | hp1 | a0001 | c0001 | t0023 | g0116 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02717 | hp1 | a0001 | c0001 | t0021 | g0029 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0324 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02818 | hp1 | a0004 | c0004 | t0002 | g0225 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02895 | hp1 | a0006 | c0008 | t0007 | g0102 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0223 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0222 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02965 | hp2 | a0002 | c0002 | t0010 | g0258 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0047 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03139 | hp1 | a0007 | c0007 | t0018 | g0183 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03195 | hp1 | a0002 | c0002 | t0009 | g0262 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0072 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03486 | hp1 | a0001 | c0005 | t0027 | g0043 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0089 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03516 | hp2 | a0003 | c0003 | t0004 | g0031 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0245 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0201 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0035 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0093 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0100 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0126 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0154 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18522 | hp1 | a0002 | c0002 | t0010 | g0257 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0224 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | CHB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0329 | EAS | CHB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | CHB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18940 | hp2 | a0001 | c0001 | t0024 | g0299 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18969 | hp2 | a0001 | c0001 | t0028 | g0310 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18987 | hp1 | a0001 | c0001 | t0012 | g0265 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18998 | hp2 | a0001 | c0001 | t0020 | g0301 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18999 | hp2 | a0001 | c0001 | t0014 | g0237 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | LWK | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0187 | AFR | LWK | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19067 | hp2 | a0001 | c0001 | t0019 | g0269 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19083 | hp1 | a0001 | c0001 | t0012 | g0251 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ASW | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ASW | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0254 | EUR | TSI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0327 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02486 | hp1 | a0002 | c0002 | t0009 | g0260 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0326 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0108 | AFR | USA | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | USA | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | USA | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | USA | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0082 | REF | REF | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0001 | REF | REF | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:110985104 | C | G | 1 | a0003 | 4 | HG01884.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
missense_variant | MODERATE | c.122C>G | p.Ala41Gly | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/10 | 191/3671 | 122/921 | 41/306 | chr6 | 110985104 | |||
| chr6:110985106 | A | C | 1 | a0005 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.124A>C | p.Asn42His | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/10 | 193/3671 | 124/921 | 42/306 | chr6 | 110985106 | |||
| chr6:110989049 | G | A | 1 | a0002 | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
missense_variant | MODERATE | c.178G>A | p.Gly60Ser | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/10 | 247/3671 | 178/921 | 60/306 | chr6 | 110989049 | |||
| chr6:111015836 | G | T | 1 | a0004 | 2 | HG02055.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.576G>T | p.Lys192Asn | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/10 | 645/3671 | 576/921 | 192/306 | chr6 | 111015836 | |||
| chr6:111025538 | A | G | 1 | a0006 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.877A>G | p.Thr293Ala | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 946/3671 | 877/921 | 293/306 | chr6 | 111025538 | |||
| chr6:111025571 | A | T | 1 | a0007 | 1 | HG03139.hp1 | stop_gained | HIGH | c.910A>T | p.Lys304* | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 979/3671 | 910/921 | 304/306 | chr6 | 111025571 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:110985054 | G | A | 1 | a0001c0005 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.72G>A | p.Pro24Pro | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/10 | 141/3671 | 72/921 | 24/306 | chr6 | 110985054 | |||
| chr6:111025498 | G | A | 1 | a0001c0006 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.837G>A | p.Arg279Arg | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 906/3671 | 837/921 | 279/306 | chr6 | 111025498 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:110982051 | T | C | 2 | a0002c0002t0009 a0002c0002t0010 |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-56T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/10 | 56 | chr6 | 110982051 | ||||||
| chr6:110982059 | G | T | 1 | a0001c0001t0028 | 1 | NA18969.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/10 | 48 | chr6 | 110982059 | ||||||
| chr6:110982093 | A | G | 1 | a0001c0001t0015 | 2 | HG01884.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-14A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/10 | 14 | chr6 | 110982093 | ||||||
| chr6:111025603 | C | T | 10 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 others(7): Show |
74 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*21C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 21 | chr6 | 111025603 | ||||||
| chr6:111025605 | G | A | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0014 others(3): Show |
63 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 23 | chr6 | 111025605 | ||||||
| chr6:111025640 | G | A | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0014 others(3): Show |
63 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*58G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 58 | chr6 | 111025640 | ||||||
| chr6:111025808 | C | T | 1 | a0001c0001t0024 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*226C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 226 | chr6 | 111025808 | ||||||
| chr6:111025921 | G | A | 1 | a0001c0001t0011 | 2 | HG03041.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*339G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 339 | chr6 | 111025921 | ||||||
| chr6:111025936 | G | A | 1 | a0001c0001t0016 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 354 | chr6 | 111025936 | ||||||
| chr6:111025943 | C | T | 2 | a0001c0001t0007 a0006c0008t0007 |
7 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*361C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 361 | chr6 | 111025943 | ||||||
| chr6:111026017 | A | ACTTTT | 14 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(11): Show |
85 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*440dupCTTTT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 441 | INFO_REALIGN_3_PRIME | chr6 | 111026017 | |||||
| chr6:111026192 | C | T | 2 | a0001c0001t0006 a0001c0001t0023 |
9 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*610C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 610 | chr6 | 111026192 | ||||||
| chr6:111026319 | T | C | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*737T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 737 | chr6 | 111026319 | ||||||
| chr6:111026371 | C | CT | 5 | a0001c0001t0006 a0001c0001t0020 a0001c0001t0021 others(2): Show |
12 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*800dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 801 | INFO_REALIGN_3_PRIME | chr6 | 111026371 | |||||
| chr6:111026446 | C | T | 1 | a0001c0001t0019 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*864C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 864 | chr6 | 111026446 | ||||||
| chr6:111026624 | G | A | 3 | a0001c0001t0006 a0001c0001t0023 a0002c0002t0010 |
12 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1042G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1042 | chr6 | 111026624 | ||||||
| chr6:111026777 | A | C | 1 | a0001c0001t0008 | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1195A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1195 | chr6 | 111026777 | ||||||
| chr6:111026819 | A | T | 14 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(11): Show |
85 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1237A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1237 | chr6 | 111026819 | ||||||
| chr6:111026843 | G | A | 1 | a0001c0001t0017 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1261G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1261 | chr6 | 111026843 | ||||||
| chr6:111026881 | T | G | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*1299T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1299 | chr6 | 111026881 | ||||||
| chr6:111026978 | A | C | 1 | a0001c0001t0005 | 10 | HG00423.hp2 NA18612.hp2 NA18968.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1396A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1396 | chr6 | 111026978 | ||||||
| chr6:111027035 | G | A | 3 | a0001c0001t0006 a0001c0001t0021 a0001c0001t0023 |
10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1453G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1453 | chr6 | 111027035 | ||||||
| chr6:111027206 | G | A | 1 | a0001c0001t0013 | 2 | HG00741.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1624G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1624 | chr6 | 111027206 | ||||||
| chr6:111027229 | A | G | 1 | a0001c0001t0026 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1647A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1647 | chr6 | 111027229 | ||||||
| chr6:111027279 | C | A | 1 | a0001c0001t0019 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1697C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1697 | chr6 | 111027279 | ||||||
| chr6:111027280 | T | G | 1 | a0001c0001t0019 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1698T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1698 | chr6 | 111027280 | ||||||
| chr6:111027351 | C | T | 10 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 others(7): Show |
74 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1769C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1769 | chr6 | 111027351 | ||||||
| chr6:111027429 | G | C | 1 | a0001c0001t0012 | 2 | NA18987.hp1 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1847G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1847 | chr6 | 111027429 | ||||||
| chr6:111027460 | G | A | 1 | a0007c0007t0018 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1878G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1878 | chr6 | 111027460 | ||||||
| chr6:111027483 | C | A | 1 | a0001c0001t0025 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1901C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1901 | chr6 | 111027483 | ||||||
| chr6:111027590 | C | T | 1 | a0001c0001t0023 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2008C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2008 | chr6 | 111027590 | ||||||
| chr6:111027995 | T | C | 3 | a0001c0001t0006 a0001c0001t0021 a0001c0001t0023 |
10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2413T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2413 | chr6 | 111027995 | ||||||
| chr6:111028112 | A | T | 1 | a0001c0001t0014 | 2 | HG02135.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2530A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2530 | chr6 | 111028112 | ||||||
| chr6:111028248 | A | C | 5 | a0001c0001t0002 a0001c0001t0008 a0002c0002t0009 others(2): Show |
93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2666A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2666 | chr6 | 111028248 | ||||||
| chr6:111028258 | A | C | 1 | a0001c0001t0013 | 2 | HG00741.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2676A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2676 | chr6 | 111028258 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:110982276 | C | G | 1 | a0001c0001t0003g0334 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.23+147C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982276 | |||||||
| chr6:110982317 | A | C | 3 | a0001c0001t0002g0332 a0001c0001t0002g0333 a0001c0001t0003g0331 |
3 | HG00438.hp1 HG00621.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.23+188A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982317 | |||||||
| chr6:110982417 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0003g0023 |
3 | HG00099.hp1 HG01169.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.23+288G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982417 | |||||||
| chr6:110982539 | A | G | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+410A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982539 | |||||||
| chr6:110982681 | C | T | 1 | a0001c0001t0002g0330 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.23+552C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982681 | |||||||
| chr6:110982700 | A | G | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+571A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982700 | |||||||
| chr6:110982733 | C | G | 2 | a0001c0001t0005g0328 a0001c0001t0005g0329 |
2 | NA18612.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.23+604C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982733 | |||||||
| chr6:110982771 | A | G | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+642A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982771 | |||||||
| chr6:110982868 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0189 |
3 | HG00597.hp1 NA18940.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.23+739G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982868 | |||||||
| chr6:110982948 | T | C | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.23+819T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982948 | |||||||
| chr6:110982957 | A | G | 2 | a0001c0001t0015g0187 a0001c0001t0015g0188 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.23+828A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982957 | |||||||
| chr6:110983055 | G | T | 1 | a0001c0001t0013g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.23+926G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983055 | |||||||
| chr6:110983244 | A | G | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.23+1115A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983244 | |||||||
| chr6:110983355 | GT | G | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+1235delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110983355 | ||||||
| chr6:110983371 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0004g0026 a0001c0001t0004g0028 others(2): Show |
5 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.23+1242G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983371 | |||||||
| chr6:110983552 | C | G | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+1423C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983552 | |||||||
| chr6:110983611 | T | C | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.24-1395T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983611 | |||||||
| chr6:110983764 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.24-1242G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983764 | |||||||
| chr6:110983801 | GGGT | G | 82 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(79): Show |
87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.24-1202_24-1200del others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110983801 | ||||||
| chr6:110983803 | GT | G | 45 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0271 others(42): Show |
45 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.24-1202delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983803 | |||||||
| chr6:110983804 | T | G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0266 a0001c0001t0001g0270 others(14): Show |
17 | HG02027.hp2 HG02071.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.24-1202T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983804 | |||||||
| chr6:110983844 | A | G | 15 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(12): Show |
15 | HG01257.hp2 HG02071.hp2 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.24-1162A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983844 | |||||||
| chr6:110983856 | C | T | 1 | a0001c0001t0007g0327 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.24-1150C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983856 | |||||||
| chr6:110983902 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0004g0026 a0001c0001t0004g0028 others(2): Show |
5 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.24-1104G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983902 | |||||||
| chr6:110983921 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.24-1085C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983921 | |||||||
| chr6:110983983 | C | T | 1 | a0003c0003t0003g0185 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.24-1023C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983983 | |||||||
| chr6:110984007 | C | G | 62 | a0001c0001t0001g0019 a0001c0001t0001g0266 a0001c0001t0001g0267 others(59): Show |
62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.24-999C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984007 | |||||||
| chr6:110984084 | A | G | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.24-922A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984084 | |||||||
| chr6:110984097 | A | T | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.24-909A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984097 | |||||||
| chr6:110984252 | G | C | 1 | a0001c0001t0003g0334 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.24-754G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984252 | |||||||
| chr6:110984331 | T | TAAAGTTT others(5): Show |
1 | a0001c0001t0012g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.24-671_24-660dupGT others(10): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110984331 | ||||||
| chr6:110984334 | A | G | 62 | a0001c0001t0001g0019 a0001c0001t0001g0266 a0001c0001t0001g0267 others(59): Show |
62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.24-672A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984334 | |||||||
| chr6:110984394 | C | T | 91 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(88): Show |
97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.24-612C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984394 | |||||||
| chr6:110984482 | T | A | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.24-524T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984482 | |||||||
| chr6:110984562 | C | T | 1 | a0007c0007t0018g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.24-444C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984562 | |||||||
| chr6:110984652 | C | G | 59 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0143 others(56): Show |
62 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.24-354C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984652 | |||||||
| chr6:110984774 | A | G | 4 | a0001c0001t0003g0128 a0001c0001t0003g0129 a0001c0001t0003g0130 others(1): Show |
4 | HG02818.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-232A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984774 | |||||||
| chr6:110984789 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.24-217A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984789 | |||||||
| chr6:110984841 | A | AAAAC | 177 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(174): Show |
184 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.24-157_24-154dupCA others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110984841 | ||||||
| chr6:110984849 | C | CAAACA | 8 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(5): Show |
8 | HG02129.hp2 HG02738.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.24-154_24-153insCA others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110984849 | ||||||
| chr6:110984881 | A | AT | 91 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(88): Show |
97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.24-117dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110984881 | ||||||
| chr6:110984890 | A | T | 1 | a0001c0001t0012g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.24-116A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984890 | |||||||
| chr6:110984958 | A | T | 1 | a0001c0001t0012g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.24-48A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984958 | |||||||
| chr6:110985150 | T | A | 5 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(2): Show |
5 | HG02738.hp2 HG03579.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+12T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985150 | |||||||
| chr6:110985245 | A | G | 1 | a0001c0001t0006g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.156+107A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985245 | |||||||
| chr6:110985422 | A | T | 62 | a0001c0001t0001g0019 a0001c0001t0001g0266 a0001c0001t0001g0267 others(59): Show |
62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.156+284A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985422 | |||||||
| chr6:110985445 | A | T | 1 | a0001c0001t0012g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+307A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985445 | |||||||
| chr6:110985472 | AC | A | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+335delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985472 | |||||||
| chr6:110985544 | G | A | 3 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0006t0004g0027 |
3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.156+406G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985544 | |||||||
| chr6:110985591 | C | G | 3 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0022g0123 |
3 | HG01952.hp1 HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.156+453C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985591 | |||||||
| chr6:110985667 | C | T | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+529C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985667 | |||||||
| chr6:110985678 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.156+540G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985678 | |||||||
| chr6:110985767 | G | A | 15 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0109 others(12): Show |
16 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+629G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985767 | |||||||
| chr6:110985794 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.156+656C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985794 | |||||||
| chr6:110985852 | C | T | 1 | a0001c0001t0003g0181 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.156+714C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985852 | |||||||
| chr6:110985885 | T | C | 185 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(182): Show |
192 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.156+747T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985885 | |||||||
| chr6:110985886 | C | G | 1 | a0001c0001t0012g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+748C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985886 | |||||||
| chr6:110985886 | C | T | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.156+748C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985886 | |||||||
| chr6:110985887 | G | A | 1 | a0001c0001t0012g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+749G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985887 | |||||||
| chr6:110985901 | G | GCA | 186 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(183): Show |
193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.156+764_156+765ins others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110985901 | ||||||
| chr6:110985903 | T | A | 1 | a0001c0001t0012g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+765T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985903 | |||||||
| chr6:110985934 | TC | T | 4 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0021g0029 others(1): Show |
4 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+797delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985934 | |||||||
| chr6:110985935 | C | CA | 88 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0143 others(85): Show |
92 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.156+815dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110985935 | ||||||
| chr6:110985935 | CA | C | 26 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0279 others(23): Show |
26 | HG01433.hp2 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.156+815delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110985935 | ||||||
| chr6:110985935 | CAA | C | 14 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0109 others(11): Show |
15 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.156+814_156+815del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110985935 | ||||||
| chr6:110986204 | A | T | 1 | a0001c0001t0012g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+1066A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986204 | |||||||
| chr6:110986229 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.156+1091C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986229 | |||||||
| chr6:110986235 | A | G | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1097A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986235 | |||||||
| chr6:110986293 | G | A | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.156+1155G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986293 | |||||||
| chr6:110986410 | A | G | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.156+1272A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986410 | |||||||
| chr6:110986424 | A | G | 4 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+1286A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986424 | |||||||
| chr6:110986474 | C | T | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+1336C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986474 | |||||||
| chr6:110986494 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0021g0029 |
2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.156+1356T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986494 | |||||||
| chr6:110986531 | G | A | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1393G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986531 | |||||||
| chr6:110986650 | T | A | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1512T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986650 | |||||||
| chr6:110986651 | A | G | 91 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(88): Show |
97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.156+1513A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986651 | |||||||
| chr6:110986680 | A | G | 181 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(178): Show |
187 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.156+1542A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986680 | |||||||
| chr6:110986720 | G | A | 1 | a0001c0001t0003g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.156+1582G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986720 | |||||||
| chr6:110986769 | C | T | 11 | a0001c0001t0001g0173 a0001c0001t0001g0178 a0001c0001t0001g0180 others(8): Show |
12 | HG00639.hp2 HG01243.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+1631C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986769 | |||||||
| chr6:110986811 | C | G | 187 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(184): Show |
194 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.156+1673C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986811 | |||||||
| chr6:110986858 | C | A | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1720C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986858 | |||||||
| chr6:110986868 | G | C | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.156+1730G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986868 | |||||||
| chr6:110986872 | G | A | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.156+1734G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986872 | |||||||
| chr6:110986930 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.156+1792C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986930 | |||||||
| chr6:110986971 | A | G | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.156+1833A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986971 | |||||||
| chr6:110986971 | A | T | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1833A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986971 | |||||||
| chr6:110987208 | C | CACCA | 3 | a0001c0001t0002g0017 a0001c0001t0002g0191 a0001c0001t0014g0192 |
4 | HG02135.hp2 NA18612.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-1819_157-1816d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110987208 | ||||||
| chr6:110987257 | C | T | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1771C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987257 | |||||||
| chr6:110987304 | C | A | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1724C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987304 | |||||||
| chr6:110987305 | C | G | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-1723C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987305 | |||||||
| chr6:110987305 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0021g0029 |
2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.157-1723C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987305 | |||||||
| chr6:110987402 | A | G | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1626A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987402 | |||||||
| chr6:110987472 | T | C | 3 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0006t0004g0027 |
3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.157-1556T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987472 | |||||||
| chr6:110987530 | A | G | 148 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(145): Show |
153 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.157-1498A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987530 | |||||||
| chr6:110987550 | A | T | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1478A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987550 | |||||||
| chr6:110987553 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.157-1475A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987553 | |||||||
| chr6:110987663 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.157-1365G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987663 | |||||||
| chr6:110987819 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.157-1209T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987819 | |||||||
| chr6:110987822 | T | G | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1206T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987822 | |||||||
| chr6:110987831 | T | G | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-1197T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987831 | |||||||
| chr6:110987868 | T | A | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-1160T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987868 | |||||||
| chr6:110987952 | T | C | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1076T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987952 | |||||||
| chr6:110987953 | G | A | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-1075G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987953 | |||||||
| chr6:110988050 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.157-978C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988050 | |||||||
| chr6:110988340 | A | G | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-688A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988340 | |||||||
| chr6:110988370 | G | A | 1 | a0001c0001t0003g0133 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.157-658G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988370 | |||||||
| chr6:110988388 | G | A | 318 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(315): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.157-640G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988388 | |||||||
| chr6:110988434 | C | CT | 6 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
7 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-577dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110988434 | ||||||
| chr6:110988434 | CTTT | C | 150 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(147): Show |
156 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.157-579_157-577del others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110988434 | ||||||
| chr6:110988552 | T | C | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-476T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988552 | |||||||
| chr6:110988648 | G | T | 62 | a0001c0001t0001g0019 a0001c0001t0001g0266 a0001c0001t0001g0267 others(59): Show |
62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.157-380G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988648 | |||||||
| chr6:110988662 | C | T | 6 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0001t0001g0083 others(3): Show |
6 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-366C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988662 | |||||||
| chr6:110988836 | A | G | 1 | a0001c0001t0003g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.157-192A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988836 | |||||||
| chr6:110989179 | TAC | T | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.194+116_194+117del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989179 | ||||||
| chr6:110989182 | A | C | 3 | a0001c0001t0002g0122 a0001c0001t0003g0120 a0001c0001t0003g0121 |
3 | HG02922.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.194+117A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989182 | |||||||
| chr6:110989201 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.194+136T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989201 | |||||||
| chr6:110989202 | C | CT | 152 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(149): Show |
158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.194+140dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989202 | ||||||
| chr6:110989202 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.194+137C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989202 | |||||||
| chr6:110989216 | G | A | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.194+151G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989216 | |||||||
| chr6:110989225 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.194+160A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989225 | |||||||
| chr6:110989476 | C | T | 59 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0143 others(56): Show |
62 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.194+411C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989476 | |||||||
| chr6:110989477 | G | A | 153 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.194+412G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989477 | |||||||
| chr6:110989482 | C | T | 1 | a0005c0009t0001g0077 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.194+417C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989482 | |||||||
| chr6:110989523 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.194+458T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989523 | |||||||
| chr6:110989627 | G | GT | 24 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(21): Show |
24 | HG00438.hp1 HG00544.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.194+579dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989627 | ||||||
| chr6:110989627 | GT | G | 32 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(29): Show |
33 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.194+579delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989627 | ||||||
| chr6:110989666 | G | T | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.194+601G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989666 | |||||||
| chr6:110989746 | C | T | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.194+681C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989746 | |||||||
| chr6:110989783 | C | G | 1 | a0001c0001t0008g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.194+718C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989783 | |||||||
| chr6:110989918 | C | T | 1 | a0001c0001t0011g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.194+853C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989918 | |||||||
| chr6:110989945 | C | CT | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+890dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989945 | ||||||
| chr6:110989951 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.194+886T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989951 | |||||||
| chr6:110990007 | A | G | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194+942A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990007 | |||||||
| chr6:110990218 | G | A | 15 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0109 others(12): Show |
16 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.194+1153G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990218 | |||||||
| chr6:110990227 | C | G | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0002g0309 |
3 | NA18942.hp2 NA18961.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.194+1162C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990227 | |||||||
| chr6:110990233 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.194+1168C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990233 | |||||||
| chr6:110990268 | T | TC | 186 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(183): Show |
193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.194+1204dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990268 | ||||||
| chr6:110990448 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0021g0029 |
2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.195-1299A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990448 | |||||||
| chr6:110990520 | T | C | 2 | a0001c0001t0004g0124 a0001c0001t0004g0125 |
2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.195-1227T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990520 | |||||||
| chr6:110990559 | A | AC | 61 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0064 others(58): Show |
67 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.195-1174dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990559 | ||||||
| chr6:110990559 | AC | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0019 others(59): Show |
65 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.195-1174delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990559 | ||||||
| chr6:110990559 | ACC | A | 44 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(41): Show |
46 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.195-1175_195-1174d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990559 | ||||||
| chr6:110990559 | ACCC | A | 48 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(45): Show |
51 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.195-1176_195-1174d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990559 | ||||||
| chr6:110990570 | C | G | 24 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0111 others(21): Show |
25 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.195-1177C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990570 | |||||||
| chr6:110990571 | C | G | 4 | a0001c0001t0001g0030 a0001c0001t0002g0109 a0001c0001t0006g0108 others(1): Show |
4 | HG01952.hp1 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-1176C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990571 | |||||||
| chr6:110990571 | CCCA | C | 24 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0111 others(21): Show |
25 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.195-1173_195-1171d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990571 | ||||||
| chr6:110990572 | C | G | 5 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0124 others(2): Show |
5 | HG00642.hp2 HG01361.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-1175C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990572 | |||||||
| chr6:110990573 | CA | C | 5 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0124 others(2): Show |
5 | HG00642.hp2 HG01361.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-1173delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990573 | |||||||
| chr6:110990576 | C | T | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-1171C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990576 | |||||||
| chr6:110990730 | GC | G | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-1014delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990730 | ||||||
| chr6:110990749 | T | A | 1 | a0001c0001t0016g0041 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.195-998T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990749 | |||||||
| chr6:110990753 | A | G | 3 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0127 |
3 | NA18943.hp2 NA19057.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.195-994A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990753 | |||||||
| chr6:110990941 | T | C | 1 | a0001c0001t0003g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.195-806T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990941 | |||||||
| chr6:110991121 | T | A | 186 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(183): Show |
193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.195-626T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991121 | |||||||
| chr6:110991353 | C | T | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-394C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991353 | |||||||
| chr6:110991373 | A | G | 187 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(184): Show |
194 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.195-374A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991373 | |||||||
| chr6:110991398 | C | CT | 31 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(28): Show |
32 | HG00621.hp2 HG00642.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.195-333dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110991398 | ||||||
| chr6:110991398 | CT | C | 6 | a0001c0001t0002g0139 a0001c0001t0002g0198 a0001c0001t0003g0013 others(3): Show |
7 | HG02602.hp1 HG03490.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.195-333delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110991398 | ||||||
| chr6:110991414 | T | A | 3 | a0001c0001t0017g0224 a0004c0004t0002g0225 a0004c0004t0002g0242 |
3 | HG02055.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.195-333T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991414 | |||||||
| chr6:110991416 | A | G | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-331A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991416 | |||||||
| chr6:110991614 | G | A | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-133G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991614 | |||||||
| chr6:110991801 | C | A | 1 | a0001c0001t0002g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.234+15C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991801 | |||||||
| chr6:110991869 | AT | A | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.234+90delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110991869 | ||||||
| chr6:110991894 | C | A | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+108C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991894 | |||||||
| chr6:110991925 | G | T | 1 | a0001c0001t0012g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.234+139G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991925 | |||||||
| chr6:110991952 | G | T | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0107 others(30): Show |
34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.234+166G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991952 | |||||||
| chr6:110991986 | T | C | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.234+200T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991986 | |||||||
| chr6:110992033 | G | A | 4 | a0001c0001t0001g0274 a0001c0001t0001g0281 a0001c0001t0001g0282 others(1): Show |
4 | NA18950.hp1 NA18964.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+247G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992033 | |||||||
| chr6:110992034 | C | T | 80 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(77): Show |
85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.234+248C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992034 | |||||||
| chr6:110992088 | C | T | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+302C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992088 | |||||||
| chr6:110992138 | C | A | 2 | a0001c0001t0003g0133 a0001c0001t0003g0153 |
2 | NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.234+352C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992138 | |||||||
| chr6:110992179 | A | G | 1 | a0001c0001t0004g0244 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.234+393A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992179 | |||||||
| chr6:110992295 | G | A | 197 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(194): Show |
204 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.234+509G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992295 | |||||||
| chr6:110992436 | A | C | 91 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(88): Show |
97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.234+650A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992436 | |||||||
| chr6:110992445 | C | CT | 7 | a0001c0001t0002g0166 a0001c0001t0002g0194 a0001c0001t0002g0221 others(4): Show |
7 | HG02132.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+674dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110992445 | ||||||
| chr6:110992445 | C | CTTTT | 14 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(11): Show |
14 | HG00642.hp2 HG01361.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.234+671_234+674dup others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110992445 | ||||||
| chr6:110992445 | C | CTTTTT | 19 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(16): Show |
20 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.234+670_234+674dup others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110992445 | ||||||
| chr6:110992445 | CT | C | 11 | a0001c0001t0001g0044 a0001c0001t0001g0173 a0001c0001t0001g0178 others(8): Show |
11 | HG00639.hp2 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+674delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110992445 | ||||||
| chr6:110992485 | C | T | 4 | a0001c0001t0003g0128 a0001c0001t0003g0129 a0001c0001t0003g0130 others(1): Show |
4 | HG02818.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+699C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992485 | |||||||
| chr6:110992493 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.234+707G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992493 | |||||||
| chr6:110992517 | A | G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
30 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.234+731A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992517 | |||||||
| chr6:110992523 | C | T | 1 | a0001c0001t0003g0062 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.234+737C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992523 | |||||||
| chr6:110992553 | C | T | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.234+767C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992553 | |||||||
| chr6:110992661 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.234+875T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992661 | |||||||
| chr6:110992695 | C | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0061 |
5 | HG01074.hp1 HG01255.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+909C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992695 | |||||||
| chr6:110992766 | T | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0272 a0001c0001t0001g0274 others(23): Show |
26 | HG00438.hp2 HG00597.hp2 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.234+980T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992766 | |||||||
| chr6:110992815 | G | A | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1029G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992815 | |||||||
| chr6:110992882 | G | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1096G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992882 | |||||||
| chr6:110992898 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.234+1112G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992898 | |||||||
| chr6:110993108 | G | A | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.234+1322G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993108 | |||||||
| chr6:110993126 | G | C | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.234+1340G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993126 | |||||||
| chr6:110993231 | C | T | 1 | a0001c0001t0014g0192 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.234+1445C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993231 | |||||||
| chr6:110993232 | G | A | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1446G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993232 | |||||||
| chr6:110993245 | A | G | 1 | a0001c0001t0002g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.234+1459A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993245 | |||||||
| chr6:110993257 | TTTG | T | 3 | a0003c0003t0003g0032 a0003c0003t0003g0185 a0003c0003t0004g0031 |
3 | HG02258.hp1 HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.234+1480_234+1482d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110993257 | ||||||
| chr6:110993265 | TG | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1480delG | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993265 | |||||||
| chr6:110993300 | GT | G | 186 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(183): Show |
193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.234+1523delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110993300 | ||||||
| chr6:110993354 | A | T | 257 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(254): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.234+1568A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993354 | |||||||
| chr6:110993537 | A | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1751A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993537 | |||||||
| chr6:110993714 | A | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1928A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993714 | |||||||
| chr6:110993969 | T | C | 1 | a0007c0007t0018g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.234+2183T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993969 | |||||||
| chr6:110993975 | C | T | 2 | a0002c0002t0009g0260 a0002c0002t0009g0261 |
2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.234+2189C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993975 | |||||||
| chr6:110994003 | A | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+2217A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994003 | |||||||
| chr6:110994029 | C | G | 1 | a0001c0001t0003g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.234+2243C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994029 | |||||||
| chr6:110994029 | C | T | 23 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(20): Show |
24 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.234+2243C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994029 | |||||||
| chr6:110994058 | C | G | 2 | a0001c0001t0004g0124 a0001c0001t0004g0125 |
2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.234+2272C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994058 | |||||||
| chr6:110994112 | A | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(5): Show |
8 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+2326A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994112 | |||||||
| chr6:110994206 | T | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+2420T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994206 | |||||||
| chr6:110994278 | TA | T | 178 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(175): Show |
184 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.234+2506delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994278 | ||||||
| chr6:110994412 | C | T | 2 | a0001c0001t0007g0324 a0001c0001t0007g0325 |
2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.234+2626C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994412 | |||||||
| chr6:110994540 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.235-2643G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994540 | |||||||
| chr6:110994727 | G | GTATATAT others(5): Show |
38 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(35): Show |
41 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.235-2448_235-2447i others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | G | GTATATAT others(7): Show |
73 | a0001c0001t0001g0019 a0001c0001t0001g0266 a0001c0001t0001g0267 others(70): Show |
75 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.235-2448_235-2447i others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | G | GTATATAT others(9): Show |
22 | a0001c0001t0001g0272 a0001c0001t0001g0288 a0001c0001t0001g0289 others(19): Show |
22 | HG00621.hp1 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.235-2448_235-2447i others(18): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | G | GTATATAT others(11): Show |
9 | a0001c0001t0001g0107 a0001c0001t0001g0296 a0001c0001t0001g0297 others(6): Show |
9 | HG01255.hp2 HG02027.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.235-2448_235-2447i others(20): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | G | GTATATAT others(13): Show |
3 | a0001c0001t0001g0294 a0001c0001t0002g0122 a0001c0001t0003g0121 |
3 | HG03098.hp1 HG03486.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.235-2448_235-2447i others(22): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | G | GTATATAT others(15): Show |
1 | a0001c0001t0002g0106 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(24): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | G | GTATATAT others(17): Show |
2 | a0001c0001t0002g0105 a0001c0001t0005g0104 |
2 | NA18968.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.235-2448_235-2447i others(26): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | G | GTATATAT others(31): Show |
1 | a0002c0002t0010g0259 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(40): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | G | GTATATAT others(33): Show |
1 | a0002c0002t0010g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(42): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | G | GTT | 4 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0021g0029 others(1): Show |
4 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2455_235-2454i others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994727 | GTA | G | 4 | a0001c0001t0003g0128 a0001c0001t0003g0129 a0001c0001t0003g0130 others(1): Show |
4 | HG02818.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2449_235-2448d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | ||||||
| chr6:110994729 | A | T | 21 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(18): Show |
22 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.235-2454A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994729 | |||||||
| chr6:110994730 | T | TACACACA others(7): Show |
1 | a0001c0001t0003g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235-2452_235-2451i others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994730 | ||||||
| chr6:110994732 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235-2451T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994732 | |||||||
| chr6:110994732 | T | TACAC | 4 | a0001c0001t0001g0073 a0001c0001t0003g0133 a0001c0001t0003g0171 others(1): Show |
4 | HG01106.hp2 HG02572.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2450_235-2449i others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994732 | ||||||
| chr6:110994732 | T | TACACACA others(1): Show |
6 | a0001c0001t0001g0021 a0001c0001t0003g0140 a0001c0001t0003g0156 others(3): Show |
6 | HG00099.hp1 HG01891.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-2450_235-2449i others(10): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994732 | ||||||
| chr6:110994732 | T | TACACACA others(3): Show |
3 | a0001c0001t0003g0165 a0001c0001t0003g0169 a0003c0003t0004g0031 |
3 | HG02572.hp2 HG03516.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.235-2450_235-2449i others(12): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994732 | ||||||
| chr6:110994732 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0022 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.235-2450_235-2449i others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994732 | ||||||
| chr6:110994734 | T | C | 17 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0073 others(14): Show |
17 | HG00099.hp1 HG01106.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-2449T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994734 | |||||||
| chr6:110994734 | T | TAC | 4 | a0001c0001t0001g0004 a0001c0001t0001g0083 a0001c0001t0011g0047 others(1): Show |
5 | HG03041.hp1 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-2414_235-2413d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TACAC | 18 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0044 others(15): Show |
19 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.235-2416_235-2413d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TACACAC | 8 | a0001c0001t0001g0162 a0001c0001t0003g0062 a0001c0001t0003g0177 others(5): Show |
8 | HG00544.hp2 HG01109.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-2418_235-2413d others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TACACACA others(1): Show |
29 | a0001c0001t0001g0086 a0001c0001t0001g0149 a0001c0001t0001g0160 others(26): Show |
32 | HG00558.hp2 HG00639.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.235-2420_235-2413d others(10): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TACACACA others(3): Show |
10 | a0001c0001t0001g0042 a0001c0001t0001g0143 a0001c0001t0003g0132 others(7): Show |
10 | HG01346.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-2422_235-2413d others(12): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TACACACA others(5): Show |
4 | a0001c0001t0003g0058 a0001c0001t0003g0157 a0001c0001t0003g0158 others(1): Show |
4 | HG02647.hp1 HG03139.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2424_235-2413d others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TACACACA others(7): Show |
2 | a0001c0001t0003g0134 a0001c0001t0004g0136 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.235-2426_235-2413d others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TACACACA others(9): Show |
1 | a0001c0001t0004g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.235-2428_235-2413d others(18): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATACACA others(3): Show |
1 | a0001c0001t0003g0164 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(12): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATATATA others(13): Show |
1 | a0001c0001t0003g0120 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(22): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATATATA others(15): Show |
1 | a0002c0002t0009g0261 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(24): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATATATA others(25): Show |
1 | a0001c0001t0001g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(34): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATATATA others(33): Show |
1 | a0001c0001t0007g0324 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(42): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATATATA others(33): Show |
2 | a0001c0001t0007g0020 a0001c0001t0007g0326 |
3 | HG02559.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.235-2448_235-2447i others(42): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATATATA others(35): Show |
1 | a0001c0001t0007g0325 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(44): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATATATA others(35): Show |
1 | a0001c0001t0007g0327 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(44): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATATATA others(35): Show |
2 | a0002c0002t0009g0260 a0002c0002t0010g0257 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.235-2448_235-2447i others(44): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | T | TATATATA others(39): Show |
1 | a0002c0002t0009g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(48): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | TAC | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0063 others(1): Show |
4 | HG01346.hp1 HG01934.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-2414_235-2413d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | TACAC | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(21): Show |
28 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.235-2416_235-2413d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994734 | TACACACA others(7): Show |
T | 1 | a0001c0001t0004g0080 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.235-2426_235-2413d others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | ||||||
| chr6:110994736 | C | T | 167 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0107 others(164): Show |
173 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-2447C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994736 | |||||||
| chr6:110994738 | C | T | 153 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0048 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.235-2445C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994738 | |||||||
| chr6:110994740 | C | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(121): Show |
130 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.235-2443C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994740 | |||||||
| chr6:110994742 | C | T | 61 | a0001c0001t0001g0019 a0001c0001t0001g0266 a0001c0001t0001g0267 others(58): Show |
61 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.235-2441C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994742 | |||||||
| chr6:110994744 | C | T | 49 | a0001c0001t0001g0019 a0001c0001t0001g0267 a0001c0001t0001g0268 others(46): Show |
49 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.235-2439C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994744 | |||||||
| chr6:110994747 | A | ACACT | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0061 |
5 | HG01074.hp1 HG01255.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-2433_235-2432i others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994747 | ||||||
| chr6:110994759 | A | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-2424A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994759 | |||||||
| chr6:110994760 | C | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-2423C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994760 | |||||||
| chr6:110994761 | A | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-2422A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994761 | |||||||
| chr6:110994770 | C | T | 92 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0111 others(89): Show |
94 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.235-2413C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994770 | |||||||
| chr6:110994771 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.235-2412G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994771 | |||||||
| chr6:110994895 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.235-2288A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994895 | |||||||
| chr6:110994939 | C | G | 5 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 others(2): Show |
5 | NA18953.hp1 NA18975.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-2244C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994939 | |||||||
| chr6:110995017 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.235-2166A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995017 | |||||||
| chr6:110995068 | A | AT | 24 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(21): Show |
25 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.235-2107dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110995068 | ||||||
| chr6:110995144 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235-2039A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995144 | |||||||
| chr6:110995159 | C | T | 62 | a0001c0001t0001g0019 a0001c0001t0001g0266 a0001c0001t0001g0267 others(59): Show |
62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.235-2024C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995159 | |||||||
| chr6:110995270 | C | G | 1 | a0001c0001t0004g0101 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.235-1913C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995270 | |||||||
| chr6:110995283 | G | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1900G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995283 | |||||||
| chr6:110995416 | C | G | 80 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(77): Show |
85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.235-1767C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995416 | |||||||
| chr6:110995492 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.235-1691A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995492 | |||||||
| chr6:110995543 | T | C | 1 | a0001c0001t0003g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.235-1640T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995543 | |||||||
| chr6:110995587 | G | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1596G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995587 | |||||||
| chr6:110995682 | C | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1501C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995682 | |||||||
| chr6:110995803 | A | G | 1 | a0001c0001t0003g0151 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.235-1380A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995803 | |||||||
| chr6:110995841 | C | T | 1 | a0006c0008t0007g0102 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.235-1342C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995841 | |||||||
| chr6:110995868 | A | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1315A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995868 | |||||||
| chr6:110995878 | G | A | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-1305G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995878 | |||||||
| chr6:110995908 | T | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1275T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995908 | |||||||
| chr6:110995915 | C | T | 1 | a0001c0001t0004g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.235-1268C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995915 | |||||||
| chr6:110996018 | A | G | 1 | a0001c0001t0017g0224 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.235-1165A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996018 | |||||||
| chr6:110996069 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.235-1114C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996069 | |||||||
| chr6:110996092 | A | G | 1 | a0001c0001t0011g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.235-1091A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996092 | |||||||
| chr6:110996093 | C | T | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-1090C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996093 | |||||||
| chr6:110996098 | G | A | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1085G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996098 | |||||||
| chr6:110996123 | AGTT | A | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1059_235-1057d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996123 | |||||||
| chr6:110996124 | G | GT | 12 | a0001c0001t0001g0075 a0001c0001t0001g0143 a0001c0001t0001g0149 others(9): Show |
12 | HG01346.hp2 HG01433.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-1042dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110996124 | ||||||
| chr6:110996124 | GT | G | 138 | a0001c0001t0001g0019 a0001c0001t0001g0204 a0001c0001t0001g0208 others(135): Show |
144 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.235-1042delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110996124 | ||||||
| chr6:110996127 | T | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1056T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996127 | |||||||
| chr6:110996265 | G | A | 62 | a0001c0001t0001g0019 a0001c0001t0001g0266 a0001c0001t0001g0267 others(59): Show |
62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.235-918G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996265 | |||||||
| chr6:110996290 | T | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-893T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996290 | |||||||
| chr6:110996359 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.235-824A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996359 | |||||||
| chr6:110996595 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0060 a0001c0001t0001g0070 others(1): Show |
4 | HG00639.hp1 HG01106.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-588C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996595 | |||||||
| chr6:110996605 | G | A | 11 | a0001c0001t0001g0173 a0001c0001t0001g0178 a0001c0001t0001g0180 others(8): Show |
12 | HG00639.hp2 HG01243.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-578G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996605 | |||||||
| chr6:110996660 | C | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-523C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996660 | |||||||
| chr6:110996785 | T | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-398T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996785 | |||||||
| chr6:110996786 | TAG | T | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-394_235-393del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110996786 | ||||||
| chr6:110996788 | G | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-395G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996788 | |||||||
| chr6:110996790 | G | A | 1 | a0006c0008t0007g0102 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.235-393G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996790 | |||||||
| chr6:110996912 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | NA18961.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.235-271G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996912 | |||||||
| chr6:110996990 | T | C | 186 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(183): Show |
193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.235-193T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996990 | |||||||
| chr6:110997091 | G | A | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-92G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110997091 | |||||||
| chr6:110997179 | A | T | 3 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0006t0004g0027 |
3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
splice_region_variant&intron_variant | LOW | c.235-4A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110997179 | |||||||
| chr6:110997385 | A | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+121A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997385 | |||||||
| chr6:110997526 | A | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(5): Show |
8 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+262A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997526 | |||||||
| chr6:110997610 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.316+346G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997610 | |||||||
| chr6:110997684 | C | A | 1 | a0001c0001t0002g0332 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.316+420C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997684 | |||||||
| chr6:110997719 | GA | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+464delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110997719 | ||||||
| chr6:110997771 | G | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+507G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997771 | |||||||
| chr6:110997775 | T | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+511T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997775 | |||||||
| chr6:110997806 | T | A | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+542T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997806 | |||||||
| chr6:110997883 | T | C | 2 | a0004c0004t0002g0225 a0004c0004t0002g0242 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.316+619T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997883 | |||||||
| chr6:110997899 | CT | C | 82 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(79): Show |
87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.316+650delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110997899 | ||||||
| chr6:110997997 | C | T | 2 | a0001c0001t0004g0094 a0001c0001t0004g0100 |
2 | HG01070.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.316+733C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997997 | |||||||
| chr6:110998030 | G | A | 1 | a0001c0001t0003g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316+766G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998030 | |||||||
| chr6:110998173 | G | A | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+909G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998173 | |||||||
| chr6:110998383 | C | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+1119C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998383 | |||||||
| chr6:110998463 | C | G | 1 | a0001c0001t0004g0045 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.316+1199C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998463 | |||||||
| chr6:110998484 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0020g0301 |
2 | NA18992.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.316+1220C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998484 | |||||||
| chr6:110998531 | A | G | 17 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0109 others(14): Show |
18 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.317-1180A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998531 | |||||||
| chr6:110998637 | T | C | 159 | a0001c0001t0001g0019 a0001c0001t0001g0103 a0001c0001t0001g0107 others(156): Show |
165 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.317-1074T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998637 | |||||||
| chr6:110998690 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.317-1021C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998690 | |||||||
| chr6:110998710 | A | G | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.317-1001A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998710 | |||||||
| chr6:110998944 | C | CA | 13 | a0001c0001t0001g0005 a0001c0001t0001g0306 a0001c0001t0002g0250 others(10): Show |
15 | HG01175.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.317-748dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110998944 | ||||||
| chr6:110998944 | CA | C | 6 | a0001c0001t0001g0315 a0001c0001t0002g0198 a0001c0001t0002g0202 others(3): Show |
6 | HG01099.hp1 HG03239.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-748delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110998944 | ||||||
| chr6:110998944 | CAA | C | 6 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(3): Show |
6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-749_317-748del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110998944 | ||||||
| chr6:110998944 | CAAA | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.317-750_317-748del others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110998944 | ||||||
| chr6:110998963 | A | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.317-748A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998963 | |||||||
| chr6:110998980 | A | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.317-731A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998980 | |||||||
| chr6:110999105 | G | A | 4 | a0001c0001t0001g0107 a0001c0001t0002g0105 a0001c0001t0002g0106 others(1): Show |
4 | HG02738.hp2 NA18968.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-606G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999105 | |||||||
| chr6:110999139 | C | T | 4 | a0001c0001t0001g0275 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | HG00438.hp2 HG02040.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-572C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999139 | |||||||
| chr6:110999238 | C | T | 159 | a0001c0001t0001g0019 a0001c0001t0001g0103 a0001c0001t0001g0107 others(156): Show |
165 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.317-473C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999238 | |||||||
| chr6:110999348 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.317-363A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999348 | |||||||
| chr6:110999467 | C | T | 4 | a0001c0001t0002g0199 a0001c0001t0002g0203 a0001c0001t0002g0220 others(1): Show |
4 | HG00735.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-244C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999467 | |||||||
| chr6:110999493 | A | G | 1 | a0001c0001t0002g0246 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.317-218A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999493 | |||||||
| chr6:110999494 | G | A | 1 | a0001c0001t0002g0246 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.317-217G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999494 | |||||||
| chr6:110999532 | C | A | 26 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(23): Show |
27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.317-179C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999532 | |||||||
| chr6:110999591 | G | A | 85 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(82): Show |
91 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.317-120G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999591 | |||||||
| chr6:110999831 | T | A | 1 | a0001c0001t0002g0230 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.393+44T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 110999831 | |||||||
| chr6:110999834 | A | G | 185 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(182): Show |
192 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.393+47A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 110999834 | |||||||
| chr6:111000046 | G | GTTTA | 187 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0103 others(184): Show |
194 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.393+262_393+263ins others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111000046 | ||||||
| chr6:111000111 | G | A | 26 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(23): Show |
27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+324G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000111 | |||||||
| chr6:111000132 | G | A | 1 | a0001c0001t0003g0169 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.393+345G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000132 | |||||||
| chr6:111000134 | C | T | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+347C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000134 | |||||||
| chr6:111000231 | A | G | 1 | a0006c0008t0007g0102 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.393+444A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000231 | |||||||
| chr6:111000246 | AG | A | 3 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0022g0123 |
3 | HG01952.hp1 HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.393+461delG | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111000246 | ||||||
| chr6:111000495 | A | G | 1 | a0001c0001t0003g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.393+708A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000495 | |||||||
| chr6:111000724 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.393+937A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000724 | |||||||
| chr6:111000771 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | NA18961.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.393+984G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000771 | |||||||
| chr6:111000801 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.393+1014G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000801 | |||||||
| chr6:111000868 | A | ATAT | 26 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(23): Show |
27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+1082_393+1083i others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111000868 | ||||||
| chr6:111000965 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.393+1178A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000965 | |||||||
| chr6:111001218 | C | T | 26 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(23): Show |
27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+1431C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001218 | |||||||
| chr6:111001232 | A | G | 26 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(23): Show |
27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+1445A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001232 | |||||||
| chr6:111001240 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.393+1453A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001240 | |||||||
| chr6:111001258 | A | T | 1 | a0001c0001t0002g0246 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.393+1471A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001258 | |||||||
| chr6:111001310 | C | A | 26 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(23): Show |
27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+1523C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001310 | |||||||
| chr6:111001311 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+1524G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001311 | |||||||
| chr6:111001430 | C | T | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+1643C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001430 | |||||||
| chr6:111001440 | C | T | 1 | a0001c0001t0003g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.393+1653C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001440 | |||||||
| chr6:111001626 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.393+1839G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001626 | |||||||
| chr6:111001646 | A | G | 333 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(330): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.393+1859A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001646 | |||||||
| chr6:111001647 | C | G | 1 | a0001c0001t0002g0246 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.393+1860C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001647 | |||||||
| chr6:111001667 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.393+1880T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001667 | |||||||
| chr6:111001692 | C | A | 2 | a0001c0001t0003g0128 a0001c0001t0003g0130 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.393+1905C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001692 | |||||||
| chr6:111001756 | A | T | 1 | a0001c0001t0002g0246 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.393+1969A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001756 | |||||||
| chr6:111001881 | T | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0002g0109 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.393+2094T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001881 | |||||||
| chr6:111001953 | G | C | 87 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0248 others(84): Show |
93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.393+2166G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001953 | |||||||
| chr6:111001963 | G | T | 2 | a0001c0001t0002g0105 a0001c0001t0005g0104 |
2 | NA18968.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.393+2176G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001963 | |||||||
| chr6:111001984 | G | A | 2 | a0001c0001t0004g0009 a0001c0001t0004g0096 |
3 | HG00280.hp2 HG00735.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.393+2197G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001984 | |||||||
| chr6:111002018 | G | A | 1 | a0001c0001t0002g0330 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.393+2231G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002018 | |||||||
| chr6:111002022 | G | A | 1 | a0001c0001t0004g0094 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.393+2235G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002022 | |||||||
| chr6:111002064 | G | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0002g0109 others(22): Show |
26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.393+2277G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002064 | |||||||
| chr6:111002085 | A | G | 191 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(188): Show |
198 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.393+2298A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002085 | |||||||
| chr6:111002295 | A | AAATAAT | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+2510_393+2511i others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111002295 | ||||||
| chr6:111002375 | C | T | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+2588C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002375 | |||||||
| chr6:111002533 | A | G | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.393+2746A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002533 | |||||||
| chr6:111002769 | C | G | 67 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(64): Show |
72 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.393+2982C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002769 | |||||||
| chr6:111002773 | C | CT | 46 | a0001c0001t0001g0208 a0001c0001t0001g0248 a0001c0001t0001g0256 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.393+2998dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111002773 | ||||||
| chr6:111002773 | C | CTT | 89 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(86): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.393+2997_393+2998d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111002773 | ||||||
| chr6:111002773 | CT | C | 44 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0016 others(41): Show |
46 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.393+2998delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111002773 | ||||||
| chr6:111002837 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.393+3050C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002837 | |||||||
| chr6:111003009 | G | A | 2 | a0001c0001t0015g0187 a0001c0001t0015g0188 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.393+3222G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003009 | |||||||
| chr6:111003046 | G | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3259G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003046 | |||||||
| chr6:111003052 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.393+3265G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003052 | |||||||
| chr6:111003079 | A | AC | 40 | a0001c0001t0001g0248 a0001c0001t0002g0016 a0001c0001t0002g0017 others(37): Show |
42 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.393+3302dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111003079 | ||||||
| chr6:111003079 | ACC | A | 88 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(85): Show |
89 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.393+3301_393+3302d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111003079 | ||||||
| chr6:111003081 | C | G | 1 | a0001c0001t0008g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+3294C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003081 | |||||||
| chr6:111003082 | C | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0149 |
2 | HG01346.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.393+3295C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003082 | |||||||
| chr6:111003090 | T | C | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0226 |
3 | HG01081.hp2 HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.393+3303T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003090 | |||||||
| chr6:111003171 | T | C | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.393+3384T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003171 | |||||||
| chr6:111003292 | T | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3505T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003292 | |||||||
| chr6:111003351 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.393+3564C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003351 | |||||||
| chr6:111003354 | G | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3567G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003354 | |||||||
| chr6:111003376 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0002g0249 |
2 | NA19058.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.393+3589C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003376 | |||||||
| chr6:111003447 | T | C | 189 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(186): Show |
196 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.393+3660T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003447 | |||||||
| chr6:111003474 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.393+3687G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003474 | |||||||
| chr6:111003546 | A | G | 2 | a0001c0001t0002g0235 a0001c0001t0002g0330 |
2 | NA18953.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.393+3759A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003546 | |||||||
| chr6:111003552 | G | C | 9 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(6): Show |
9 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+3765G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003552 | |||||||
| chr6:111003604 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3817T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003604 | |||||||
| chr6:111003608 | A | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3821A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003608 | |||||||
| chr6:111003615 | GAAGT | G | 5 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 others(2): Show |
5 | NA18953.hp1 NA18975.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+3832_393+3835d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111003615 | ||||||
| chr6:111003651 | G | A | 12 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(9): Show |
13 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.393+3864G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003651 | |||||||
| chr6:111003694 | T | C | 25 | a0001c0001t0001g0055 a0001c0001t0001g0168 a0001c0001t0001g0182 others(22): Show |
25 | HG01257.hp2 HG02074.hp1 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.393+3907T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003694 | |||||||
| chr6:111003858 | A | G | 109 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(106): Show |
111 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.393+4071A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003858 | |||||||
| chr6:111003874 | G | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+4087G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003874 | |||||||
| chr6:111003935 | T | C | 90 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(87): Show |
91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.394-4103T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003935 | |||||||
| chr6:111004011 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-4027T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004011 | |||||||
| chr6:111004032 | C | T | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.394-4006C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004032 | |||||||
| chr6:111004033 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-4005A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004033 | |||||||
| chr6:111004268 | C | T | 4 | a0001c0001t0001g0284 a0001c0001t0001g0289 a0001c0001t0001g0292 others(1): Show |
4 | NA18959.hp2 NA18973.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-3770C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004268 | |||||||
| chr6:111004284 | G | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-3754G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004284 | |||||||
| chr6:111004306 | C | T | 1 | a0001c0001t0004g0045 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394-3732C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004306 | |||||||
| chr6:111004333 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.394-3705C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004333 | |||||||
| chr6:111004398 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-3640A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004398 | |||||||
| chr6:111004429 | A | C | 1 | a0001c0001t0002g0246 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.394-3609A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004429 | |||||||
| chr6:111004430 | C | A | 1 | a0001c0001t0002g0246 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.394-3608C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004430 | |||||||
| chr6:111004476 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.394-3562C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004476 | |||||||
| chr6:111004481 | C | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-3557C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004481 | |||||||
| chr6:111004549 | G | GT | 7 | a0001c0001t0001g0075 a0001c0001t0002g0017 a0001c0001t0002g0105 others(4): Show |
8 | HG02055.hp1 HG03831.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-3476dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111004549 | ||||||
| chr6:111004549 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.394-3489G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004549 | |||||||
| chr6:111004549 | GT | G | 89 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(86): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.394-3476delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111004549 | ||||||
| chr6:111004605 | G | A | 80 | a0001c0001t0001g0208 a0001c0001t0001g0248 a0001c0001t0001g0256 others(77): Show |
85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.394-3433G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004605 | |||||||
| chr6:111004907 | A | G | 1 | a0001c0001t0005g0302 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.394-3131A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004907 | |||||||
| chr6:111004917 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-3121T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004917 | |||||||
| chr6:111005060 | C | T | 2 | a0001c0001t0003g0128 a0001c0001t0003g0130 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.394-2978C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005060 | |||||||
| chr6:111005069 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2969T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005069 | |||||||
| chr6:111005134 | T | G | 2 | a0001c0001t0001g0042 a0001c0005t0027g0043 |
2 | HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.394-2904T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005134 | |||||||
| chr6:111005176 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.394-2862C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005176 | |||||||
| chr6:111005246 | C | T | 2 | a0001c0001t0011g0047 a0001c0001t0011g0072 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.394-2792C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005246 | |||||||
| chr6:111005521 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2517A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005521 | |||||||
| chr6:111005533 | G | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2505G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005533 | |||||||
| chr6:111005582 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2456A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005582 | |||||||
| chr6:111005720 | C | T | 2 | a0001c0001t0003g0058 a0001c0001t0003g0138 |
2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.394-2318C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005720 | |||||||
| chr6:111005723 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2315T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005723 | |||||||
| chr6:111005884 | T | G | 69 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(66): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.394-2154T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005884 | |||||||
| chr6:111006130 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.394-1908C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006130 | |||||||
| chr6:111006140 | A | G | 110 | a0001c0001t0001g0042 a0001c0001t0001g0103 a0001c0001t0001g0107 others(107): Show |
116 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.394-1898A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006140 | |||||||
| chr6:111006169 | G | A | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.394-1869G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006169 | |||||||
| chr6:111006194 | G | C | 72 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(69): Show |
72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.394-1844G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006194 | |||||||
| chr6:111006241 | A | ATT | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1788_394-1787d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111006241 | ||||||
| chr6:111006267 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.394-1771C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006267 | |||||||
| chr6:111006304 | G | A | 1 | a0006c0008t0007g0102 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.394-1734G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006304 | |||||||
| chr6:111006479 | GC | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1555delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111006479 | ||||||
| chr6:111006558 | C | A | 1 | a0001c0001t0002g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.394-1480C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006558 | |||||||
| chr6:111006559 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.394-1479T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006559 | |||||||
| chr6:111006562 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.394-1476T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006562 | |||||||
| chr6:111006685 | G | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1353G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006685 | |||||||
| chr6:111006732 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0300 |
2 | NA19057.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.394-1306G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006732 | |||||||
| chr6:111006765 | C | G | 80 | a0001c0001t0001g0208 a0001c0001t0001g0248 a0001c0001t0001g0256 others(77): Show |
85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.394-1273C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006765 | |||||||
| chr6:111006782 | A | G | 14 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(11): Show |
15 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-1256A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006782 | |||||||
| chr6:111006802 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1236A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006802 | |||||||
| chr6:111006845 | G | A | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.394-1193G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006845 | |||||||
| chr6:111006878 | G | A | 191 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(188): Show |
198 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.394-1160G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006878 | |||||||
| chr6:111006903 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1135A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006903 | |||||||
| chr6:111006924 | T | C | 1 | a0001c0001t0003g0062 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.394-1114T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006924 | |||||||
| chr6:111006933 | C | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1105C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006933 | |||||||
| chr6:111007123 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-915T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007123 | |||||||
| chr6:111007169 | C | T | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-869C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007169 | |||||||
| chr6:111007308 | C | T | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.394-730C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007308 | |||||||
| chr6:111007442 | C | T | 1 | a0006c0008t0007g0102 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.394-596C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007442 | |||||||
| chr6:111007470 | T | G | 6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-568T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007470 | |||||||
| chr6:111007475 | G | T | 1 | a0001c0001t0003g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.394-563G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007475 | |||||||
| chr6:111007604 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.394-434A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007604 | |||||||
| chr6:111007632 | G | A | 2 | a0001c0001t0003g0157 a0001c0001t0003g0211 |
2 | HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.394-406G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007632 | |||||||
| chr6:111007813 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.394-225G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007813 | |||||||
| chr6:111007861 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-177T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007861 | |||||||
| chr6:111007909 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.394-129T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007909 | |||||||
| chr6:111008018 | C | CT | 6 | a0001c0001t0001g0038 a0001c0001t0002g0196 a0001c0001t0002g0210 others(3): Show |
6 | HG02135.hp2 HG02717.hp1 NA19067.hp1 others(3): Show |
splice_acceptor_variant&intron_variant | HIGH | c.394-3dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111008018 | ||||||
| chr6:111008018 | CT | C | 89 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0030 others(86): Show |
90 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
splice_region_variant&intron_variant | LOW | c.394-3delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111008018 | ||||||
| chr6:111008167 | G | T | 3 | a0001c0001t0006g0012 a0001c0001t0006g0115 a0001c0001t0023g0116 |
4 | HG01168.hp2 HG01192.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+30G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008167 | |||||||
| chr6:111008306 | C | T | 13 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0109 others(10): Show |
14 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+169C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008306 | |||||||
| chr6:111008420 | T | TC | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+286dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008420 | ||||||
| chr6:111008557 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+420A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008557 | |||||||
| chr6:111008624 | T | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+487T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008624 | |||||||
| chr6:111008799 | A | G | 1 | a0001c0001t0001g0320 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.493+662A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008799 | |||||||
| chr6:111008810 | G | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+673G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008810 | |||||||
| chr6:111008898 | C | CTT | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+778_493+779dup others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | C | CTTTTTTT others(5): Show |
6 | a0002c0002t0009g0260 a0002c0002t0009g0261 a0002c0002t0009g0262 others(3): Show |
6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+768_493+779dup others(12): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.493+766_493+779dup others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | C | CTTTTTTT others(8): Show |
18 | a0001c0001t0002g0017 a0001c0001t0002g0184 a0001c0001t0002g0189 others(15): Show |
19 | HG00423.hp1 HG00609.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.493+765_493+779dup others(15): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | C | CTTTTTTT others(9): Show |
27 | a0001c0001t0001g0256 a0001c0001t0002g0003 a0001c0001t0002g0016 others(24): Show |
30 | HG00558.hp1 HG00597.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+764_493+779dup others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | C | CTTTTTTT others(10): Show |
18 | a0001c0001t0001g0208 a0001c0001t0001g0248 a0001c0001t0002g0205 others(15): Show |
18 | HG00438.hp1 HG00621.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.493+763_493+779dup others(17): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | C | CTTTTTTT others(11): Show |
12 | a0001c0001t0002g0018 a0001c0001t0002g0194 a0001c0001t0002g0209 others(9): Show |
13 | HG00140.hp2 HG00280.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.493+762_493+779dup others(18): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0110 a0001c0001t0002g0254 a0004c0004t0002g0242 |
3 | HG02055.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.493+779_493+780ins others(19): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | C | CTTTTTTT others(13): Show |
5 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0122 others(2): Show |
5 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+779_493+780ins others(20): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.493+779_493+780ins others(24): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | CT | C | 17 | a0001c0001t0001g0051 a0001c0001t0003g0128 a0001c0001t0003g0129 others(14): Show |
17 | HG01515.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.493+779delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008898 | CTTTTTTT others(1): Show |
C | 90 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(87): Show |
91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.493+772_493+779del others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | ||||||
| chr6:111008923 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+786A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008923 | |||||||
| chr6:111008968 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.493+831C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008968 | |||||||
| chr6:111009094 | C | T | 92 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(89): Show |
93 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.493+957C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009094 | |||||||
| chr6:111009296 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(21): Show |
28 | HG00099.hp2 HG00609.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.493+1159C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009296 | |||||||
| chr6:111009297 | A | G | 314 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(311): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.493+1160A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009297 | |||||||
| chr6:111009306 | G | A | 80 | a0001c0001t0001g0208 a0001c0001t0001g0248 a0001c0001t0001g0256 others(77): Show |
85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.493+1169G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009306 | |||||||
| chr6:111009392 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1255T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009392 | |||||||
| chr6:111009408 | G | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1271G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009408 | |||||||
| chr6:111009484 | C | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0063 others(2): Show |
5 | HG01346.hp1 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+1347C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009484 | |||||||
| chr6:111009524 | T | G | 1 | a0006c0008t0007g0102 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.493+1387T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009524 | |||||||
| chr6:111009907 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1770T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009907 | |||||||
| chr6:111009913 | A | G | 1 | a0006c0008t0007g0102 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.493+1776A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009913 | |||||||
| chr6:111009976 | A | G | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.493+1839A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009976 | |||||||
| chr6:111010095 | T | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1958T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010095 | |||||||
| chr6:111010109 | C | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1972C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010109 | |||||||
| chr6:111010128 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.493+1991C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010128 | |||||||
| chr6:111010128 | CTT | C | 87 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(84): Show |
88 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.493+2002_493+2003d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111010128 | ||||||
| chr6:111010129 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.493+1992T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010129 | |||||||
| chr6:111010130 | T | C | 2 | a0001c0001t0001g0323 a0001c0001t0004g0124 |
2 | HG03453.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.493+1993T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010130 | |||||||
| chr6:111010326 | G | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2189G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010326 | |||||||
| chr6:111010352 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.493+2215C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010352 | |||||||
| chr6:111010439 | G | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2302G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010439 | |||||||
| chr6:111010547 | C | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(14): Show |
18 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.493+2410C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010547 | |||||||
| chr6:111010554 | C | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2417C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010554 | |||||||
| chr6:111010574 | C | T | 1 | a0006c0008t0007g0102 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.493+2437C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010574 | |||||||
| chr6:111010652 | A | C | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.493+2515A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010652 | |||||||
| chr6:111010663 | C | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2526C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010663 | |||||||
| chr6:111010780 | A | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2643A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010780 | |||||||
| chr6:111010871 | A | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2734A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010871 | |||||||
| chr6:111010915 | G | C | 13 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0109 others(10): Show |
14 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+2778G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010915 | |||||||
| chr6:111010918 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.493+2781T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010918 | |||||||
| chr6:111011090 | G | A | 12 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(9): Show |
13 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+2953G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011090 | |||||||
| chr6:111011105 | G | A | 13 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0109 others(10): Show |
14 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+2968G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011105 | |||||||
| chr6:111011276 | T | TTTTC | 16 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0052 others(13): Show |
16 | HG01081.hp1 HG01346.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.493+3171_493+3174d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011276 | ||||||
| chr6:111011276 | TTTTC | T | 95 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0001g0208 others(92): Show |
101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.493+3171_493+3174d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011276 | ||||||
| chr6:111011276 | TTTTCTTT others(5): Show |
T | 2 | a0001c0001t0002g0234 a0001c0001t0003g0138 |
2 | HG01099.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.493+3163_493+3174d others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011276 | ||||||
| chr6:111011301 | TTTC | T | 5 | a0001c0001t0001g0300 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
5 | HG01952.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+3167_493+3169d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011301 | ||||||
| chr6:111011302 | TTC | T | 66 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(63): Show |
66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.493+3167_493+3168d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011302 | ||||||
| chr6:111011304 | C | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(14): Show |
18 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.493+3167C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011304 | |||||||
| chr6:111011305 | TTTC | T | 11 | a0001c0001t0001g0103 a0001c0001t0002g0105 a0001c0001t0002g0106 others(8): Show |
12 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.493+3171_493+3173d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011305 | ||||||
| chr6:111011308 | C | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+3171C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011308 | |||||||
| chr6:111011396 | T | TC | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+3260dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011396 | ||||||
| chr6:111011448 | G | A | 3 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0006t0004g0027 |
3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.493+3311G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011448 | |||||||
| chr6:111011493 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+3356A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011493 | |||||||
| chr6:111011581 | G | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+3444G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011581 | |||||||
| chr6:111011715 | T | A | 1 | a0001c0001t0004g0026 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.493+3578T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011715 | |||||||
| chr6:111011744 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0004g0026 a0001c0001t0004g0028 others(1): Show |
4 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+3607T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011744 | |||||||
| chr6:111011984 | A | C | 2 | a0001c0001t0015g0187 a0001c0001t0015g0188 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.494-3770A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011984 | |||||||
| chr6:111012057 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3697A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012057 | |||||||
| chr6:111012070 | C | CT | 79 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(76): Show |
79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.494-3670dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012070 | ||||||
| chr6:111012070 | CT | C | 15 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0107 others(12): Show |
16 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.494-3670delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012070 | ||||||
| chr6:111012107 | T | C | 1 | a0001c0001t0002g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.494-3647T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012107 | |||||||
| chr6:111012139 | T | A | 1 | a0001c0001t0002g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.494-3615T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012139 | |||||||
| chr6:111012162 | A | AT | 21 | a0001c0001t0001g0052 a0001c0001t0001g0117 a0001c0001t0002g0109 others(18): Show |
23 | HG00735.hp2 HG01081.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.494-3577dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | ||||||
| chr6:111012162 | A | ATTT | 8 | a0001c0001t0001g0277 a0001c0001t0001g0311 a0001c0001t0001g0312 others(5): Show |
8 | HG00621.hp2 HG02717.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.494-3579_494-3577d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | ||||||
| chr6:111012162 | A | ATTTT | 54 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(51): Show |
54 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.494-3580_494-3577d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | ||||||
| chr6:111012162 | A | ATTTTT | 12 | a0001c0001t0001g0182 a0001c0001t0001g0266 a0001c0001t0001g0270 others(9): Show |
12 | HG02027.hp2 HG02074.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.494-3581_494-3577d others(7): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | ||||||
| chr6:111012162 | AT | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0003g0161 others(4): Show |
8 | HG02055.hp1 HG02818.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-3577delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | ||||||
| chr6:111012178 | C | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3576C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012178 | |||||||
| chr6:111012320 | G | A | 1 | a0003c0003t0004g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.494-3434G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012320 | |||||||
| chr6:111012386 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.494-3368G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012386 | |||||||
| chr6:111012414 | C | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3340C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012414 | |||||||
| chr6:111012418 | A | G | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.494-3336A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012418 | |||||||
| chr6:111012506 | G | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3248G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012506 | |||||||
| chr6:111012690 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3064A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012690 | |||||||
| chr6:111012773 | G | A | 7 | a0001c0001t0002g0200 a0001c0001t0002g0202 a0001c0001t0008g0201 others(4): Show |
7 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-2981G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012773 | |||||||
| chr6:111012866 | C | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-2888C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012866 | |||||||
| chr6:111012885 | G | T | 1 | a0001c0001t0004g0079 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.494-2869G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012885 | |||||||
| chr6:111013614 | C | T | 2 | a0004c0004t0002g0225 a0004c0004t0002g0242 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.494-2140C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111013614 | |||||||
| chr6:111013796 | TATG | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0248 a0001c0001t0002g0003 |
5 | NA18954.hp1 NA18964.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-1955_494-1953d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111013796 | ||||||
| chr6:111013874 | A | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-1880A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111013874 | |||||||
| chr6:111013875 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-1879A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111013875 | |||||||
| chr6:111014014 | T | A | 8 | a0001c0001t0001g0274 a0001c0001t0001g0281 a0001c0001t0001g0282 others(5): Show |
8 | NA18612.hp2 NA18950.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-1740T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014014 | |||||||
| chr6:111014034 | G | GT | 43 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0168 others(40): Show |
43 | HG00438.hp2 HG00597.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.494-1708dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111014034 | ||||||
| chr6:111014094 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.494-1660C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014094 | |||||||
| chr6:111014113 | A | C | 100 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0037 others(97): Show |
102 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.494-1641A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014113 | |||||||
| chr6:111014141 | G | GT | 16 | a0001c0001t0001g0048 a0001c0001t0002g0046 a0001c0001t0002g0105 others(13): Show |
16 | HG01433.hp2 HG02622.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.494-1600dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111014141 | ||||||
| chr6:111014147 | T | TC | 93 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0037 others(90): Show |
94 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.494-1607_494-1606i others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014147 | |||||||
| chr6:111014148 | T | C | 1 | a0001c0001t0001g0323 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.494-1606T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014148 | |||||||
| chr6:111014180 | A | G | 71 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0208 others(68): Show |
76 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.494-1574A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014180 | |||||||
| chr6:111014206 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.494-1548G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014206 | |||||||
| chr6:111014345 | T | G | 100 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0037 others(97): Show |
101 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.494-1409T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014345 | |||||||
| chr6:111014368 | A | G | 321 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(318): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.494-1386A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014368 | |||||||
| chr6:111014484 | G | A | 80 | a0001c0001t0001g0208 a0001c0001t0001g0248 a0001c0001t0001g0256 others(77): Show |
85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.494-1270G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014484 | |||||||
| chr6:111014485 | C | T | 318 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(315): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.494-1269C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014485 | |||||||
| chr6:111014852 | G | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.494-902G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014852 | |||||||
| chr6:111015021 | G | A | 94 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(91): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.494-733G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015021 | |||||||
| chr6:111015025 | G | A | 5 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(2): Show |
5 | HG02738.hp2 HG03579.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-729G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015025 | |||||||
| chr6:111015051 | G | T | 94 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(91): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.494-703G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015051 | |||||||
| chr6:111015112 | A | G | 3 | a0001c0001t0002g0122 a0001c0001t0003g0120 a0001c0001t0003g0121 |
3 | HG02922.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.494-642A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015112 | |||||||
| chr6:111015181 | AATGCTCT others(11): Show |
A | 1 | a0001c0001t0020g0301 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.494-572_494-555del others(18): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015181 | |||||||
| chr6:111015200 | G | A | 5 | a0001c0001t0022g0123 a0002c0002t0009g0262 a0002c0002t0010g0257 others(2): Show |
5 | HG01433.hp2 HG01952.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-554G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015200 | |||||||
| chr6:111015225 | A | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(5): Show |
8 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-529A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015225 | |||||||
| chr6:111015232 | A | C | 94 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(91): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.494-522A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015232 | |||||||
| chr6:111015347 | T | C | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.494-407T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015347 | |||||||
| chr6:111015414 | G | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.494-340G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015414 | |||||||
| chr6:111015564 | C | A | 5 | a0001c0001t0003g0129 a0001c0001t0003g0140 a0003c0003t0003g0032 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-190C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015564 | |||||||
| chr6:111015715 | T | A | 2 | a0001c0001t0012g0251 a0001c0001t0012g0265 |
2 | NA18987.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.494-39T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015715 | |||||||
| chr6:111015875 | A | G | 24 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(21): Show |
26 | HG00099.hp2 HG00609.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.596+19A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111015875 | |||||||
| chr6:111015970 | A | C | 1 | a0001c0001t0002g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.596+114A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111015970 | |||||||
| chr6:111016245 | A | C | 1 | a0001c0001t0004g0096 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.596+389A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016245 | |||||||
| chr6:111016302 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+446T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016302 | |||||||
| chr6:111016341 | T | C | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+485T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016341 | |||||||
| chr6:111016565 | C | G | 6 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(3): Show |
6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+709C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016565 | |||||||
| chr6:111016590 | G | C | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+734G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016590 | |||||||
| chr6:111016593 | G | GA | 35 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0001c0001t0001g0057 others(32): Show |
36 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.596+743dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016593 | ||||||
| chr6:111016593 | G | GAA | 38 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0055 others(35): Show |
38 | HG01257.hp2 HG01891.hp1 HG02040.hp1 others(35): Show |
intron_variant | MODIFIER | c.596+742_596+743dup others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016593 | ||||||
| chr6:111016593 | G | GAAA | 13 | a0001c0001t0001g0285 a0001c0001t0001g0287 a0001c0001t0001g0293 others(10): Show |
13 | HG00438.hp2 HG00597.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.596+741_596+743dup others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016593 | ||||||
| chr6:111016600 | C | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+744C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016600 | |||||||
| chr6:111016607 | C | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+751C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016607 | |||||||
| chr6:111016610 | A | AC | 3 | a0001c0001t0004g0136 a0001c0001t0004g0141 a0001c0001t0021g0029 |
3 | HG02615.hp2 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.596+754_596+755ins others(1): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016610 | |||||||
| chr6:111016638 | T | TAAAGAGT others(3138): Show |
1 | a0001c0001t0020g0301 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.596+796_596+797ins others(3145): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016638 | ||||||
| chr6:111016670 | C | CT | 9 | a0001c0001t0001g0040 a0001c0001t0022g0123 a0002c0002t0009g0262 others(6): Show |
9 | HG01433.hp2 HG01952.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.596+826dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016670 | ||||||
| chr6:111016670 | CT | C | 96 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(93): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.596+826delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016670 | ||||||
| chr6:111016680 | T | TTTTC | 6 | a0001c0001t0002g0221 a0001c0001t0007g0020 a0001c0001t0007g0324 others(3): Show |
7 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.596+826_596+827ins others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016680 | ||||||
| chr6:111016681 | T | TTTC | 80 | a0001c0001t0001g0208 a0001c0001t0001g0248 a0001c0001t0001g0256 others(77): Show |
85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.596+826_596+827ins others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016681 | ||||||
| chr6:111016683 | C | T | 101 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0103 others(98): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.596+827C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016683 | |||||||
| chr6:111016684 | T | C | 6 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(3): Show |
6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+828T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016684 | |||||||
| chr6:111016684 | TTTC | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0117 others(14): Show |
18 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.596+831_596+833del others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016684 | ||||||
| chr6:111016685 | TTC | T | 77 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(74): Show |
77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.596+831_596+832del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016685 | ||||||
| chr6:111016687 | C | T | 108 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0103 others(105): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.596+831C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016687 | |||||||
| chr6:111016688 | T | C | 1 | a0006c0008t0007g0102 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.596+832T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016688 | |||||||
| chr6:111016755 | G | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+899G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016755 | |||||||
| chr6:111016828 | C | A | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0066 others(2): Show |
5 | HG00544.hp1 HG00544.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+972C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016828 | |||||||
| chr6:111016891 | A | G | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1035A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016891 | |||||||
| chr6:111016947 | C | G | 1 | a0001c0001t0012g0251 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.596+1091C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016947 | |||||||
| chr6:111016967 | A | G | 1 | a0001c0001t0006g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.596+1111A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016967 | |||||||
| chr6:111017020 | C | G | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.596+1164C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017020 | |||||||
| chr6:111017077 | A | C | 77 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(74): Show |
77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.596+1221A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017077 | |||||||
| chr6:111017209 | A | AT | 5 | a0001c0001t0001g0288 a0001c0001t0001g0314 a0001c0001t0001g0317 others(2): Show |
5 | HG00423.hp2 NA18956.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+1353_596+1354i others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017209 | |||||||
| chr6:111017210 | C | CG | 30 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0075 others(27): Show |
30 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.596+1358dupG | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017210 | ||||||
| chr6:111017210 | C | G | 5 | a0001c0001t0001g0288 a0001c0001t0001g0314 a0001c0001t0001g0317 others(2): Show |
5 | HG00423.hp2 NA18956.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+1354C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017210 | |||||||
| chr6:111017210 | C | T | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(88): Show |
92 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.596+1354C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017210 | |||||||
| chr6:111017221 | C | G | 1 | a0001c0001t0020g0301 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.596+1365C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017221 | |||||||
| chr6:111017255 | T | C | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1399T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017255 | |||||||
| chr6:111017262 | G | A | 1 | a0004c0004t0002g0225 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.596+1406G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017262 | |||||||
| chr6:111017276 | A | C | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1420A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017276 | |||||||
| chr6:111017293 | G | A | 98 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0208 others(95): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.596+1437G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017293 | |||||||
| chr6:111017310 | G | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1454G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017310 | |||||||
| chr6:111017326 | C | T | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+1470C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017326 | |||||||
| chr6:111017336 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.596+1480G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017336 | |||||||
| chr6:111017343 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+1487C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017343 | |||||||
| chr6:111017344 | G | A | 3 | a0001c0001t0004g0136 a0001c0001t0004g0141 a0001c0001t0004g0142 |
3 | HG02109.hp2 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.596+1488G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017344 | |||||||
| chr6:111017347 | C | T | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1491C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017347 | |||||||
| chr6:111017356 | C | T | 1 | a0002c0002t0009g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.596+1500C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017356 | |||||||
| chr6:111017372 | T | C | 199 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(196): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.596+1516T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017372 | |||||||
| chr6:111017389 | AGGCGGAG others(73): Show |
A | 4 | a0001c0001t0001g0274 a0001c0001t0001g0281 a0001c0001t0001g0282 others(1): Show |
4 | NA18950.hp1 NA18964.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1541_596+1620d others(82): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017389 | ||||||
| chr6:111017391 | GCGGAGA | G | 92 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0208 others(89): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.596+1538_596+1543d others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017391 | ||||||
| chr6:111017392 | CGGAGACG others(39): Show |
C | 1 | a0001c0001t0002g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.596+1538_596+1583d others(48): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017392 | ||||||
| chr6:111017398 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.596+1542C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017398 | |||||||
| chr6:111017416 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.596+1560C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017416 | |||||||
| chr6:111017421 | C | T | 5 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0141 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+1565C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017421 | |||||||
| chr6:111017428 | C | T | 66 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(63): Show |
66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.596+1572C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017428 | |||||||
| chr6:111017431 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.596+1575A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017431 | |||||||
| chr6:111017435 | G | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.596+1579G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017435 | |||||||
| chr6:111017469 | G | A | 91 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(88): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.596+1613G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017469 | |||||||
| chr6:111017525 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+1669C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017525 | |||||||
| chr6:111017546 | G | A | 2 | a0001c0001t0015g0187 a0001c0001t0015g0188 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.596+1690G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017546 | |||||||
| chr6:111017568 | C | T | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1712C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017568 | |||||||
| chr6:111017586 | G | A | 4 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+1730G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017586 | |||||||
| chr6:111017614 | G | A | 2 | a0001c0001t0005g0328 a0001c0001t0005g0329 |
2 | NA18612.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.596+1758G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017614 | |||||||
| chr6:111017619 | G | T | 2 | a0001c0001t0004g0124 a0001c0001t0004g0125 |
2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.596+1763G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017619 | |||||||
| chr6:111017632 | C | T | 2 | a0001c0001t0005g0290 a0001c0001t0005g0304 |
2 | NA18982.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.596+1776C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017632 | |||||||
| chr6:111017670 | ACACTCCT others(33): Show |
A | 5 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0141 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+1816_596+1855d others(42): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017670 | ||||||
| chr6:111017671 | C | T | 1 | a0007c0007t0018g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.596+1815C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017671 | |||||||
| chr6:111017672 | A | G | 94 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(91): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.596+1816A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017672 | |||||||
| chr6:111017679 | A | G | 1 | a0001c0001t0002g0330 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.596+1823A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017679 | |||||||
| chr6:111017701 | C | T | 6 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(3): Show |
6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+1845C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017701 | |||||||
| chr6:111017767 | G | A | 3 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0006t0004g0027 |
3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.596+1911G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017767 | |||||||
| chr6:111017774 | A | G | 193 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(190): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.596+1918A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017774 | |||||||
| chr6:111017796 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.596+1940C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017796 | |||||||
| chr6:111017805 | C | CG | 4 | a0001c0001t0001g0069 a0001c0001t0001g0297 a0001c0001t0001g0314 others(1): Show |
4 | HG00621.hp2 HG02027.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1953dupG | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017805 | ||||||
| chr6:111017836 | T | C | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1980T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017836 | |||||||
| chr6:111017890 | G | A | 3 | a0001c0001t0017g0224 a0004c0004t0002g0225 a0004c0004t0002g0242 |
3 | HG02055.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.596+2034G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017890 | |||||||
| chr6:111017897 | C | T | 1 | a0001c0005t0027g0043 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.596+2041C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017897 | |||||||
| chr6:111017948 | C | T | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2092C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017948 | |||||||
| chr6:111017973 | G | A | 1 | a0001c0001t0004g0094 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.596+2117G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017973 | |||||||
| chr6:111017977 | G | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2121G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017977 | |||||||
| chr6:111018043 | C | T | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2187C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018043 | |||||||
| chr6:111018065 | C | A | 91 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0208 others(88): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2209C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018065 | |||||||
| chr6:111018074 | G | A | 5 | a0001c0001t0003g0129 a0001c0001t0003g0140 a0003c0003t0003g0032 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+2218G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018074 | |||||||
| chr6:111018093 | G | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2237G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018093 | |||||||
| chr6:111018127 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.596+2271C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018127 | |||||||
| chr6:111018182 | C | G | 2 | a0001c0001t0006g0012 a0001c0001t0006g0115 |
3 | HG01168.hp2 HG01192.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.596+2326C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018182 | |||||||
| chr6:111018199 | CGGGGAG | C | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+2358_596+2363d others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111018199 | ||||||
| chr6:111018200 | G | A | 1 | a0001c0001t0003g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.596+2344G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018200 | |||||||
| chr6:111018214 | G | A | 5 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0141 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+2358G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018214 | |||||||
| chr6:111018214 | G | GGAGGGAG others(5): Show |
1 | a0001c0001t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.596+2376_596+2387d others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111018214 | ||||||
| chr6:111018214 | GGAGGGA | G | 4 | a0001c0001t0001g0034 a0001c0001t0011g0047 a0001c0001t0011g0072 others(1): Show |
4 | HG02683.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+2382_596+2387d others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111018214 | ||||||
| chr6:111018245 | A | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(5): Show |
8 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.596+2389A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018245 | |||||||
| chr6:111018253 | T | A | 2 | a0001c0001t0003g0128 a0001c0001t0003g0130 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.596+2397T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018253 | |||||||
| chr6:111018344 | A | G | 2 | a0001c0001t0004g0124 a0001c0001t0004g0125 |
2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.596+2488A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018344 | |||||||
| chr6:111018496 | T | C | 82 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(79): Show |
82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.596+2640T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018496 | |||||||
| chr6:111018634 | CAG | C | 72 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(69): Show |
72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.596+2782_596+2783d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111018634 | ||||||
| chr6:111018891 | A | C | 1 | a0001c0001t0021g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.596+3035A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018891 | |||||||
| chr6:111018938 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+3082G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018938 | |||||||
| chr6:111018999 | C | T | 5 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+3143C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018999 | |||||||
| chr6:111019094 | A | T | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3238A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019094 | |||||||
| chr6:111019115 | C | G | 1 | a0001c0001t0004g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.596+3259C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019115 | |||||||
| chr6:111019169 | G | A | 6 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(3): Show |
6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+3313G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019169 | |||||||
| chr6:111019175 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+3319C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019175 | |||||||
| chr6:111019248 | G | A | 72 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(69): Show |
72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.596+3392G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019248 | |||||||
| chr6:111019287 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.596+3431G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019287 | |||||||
| chr6:111019324 | C | T | 82 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(79): Show |
82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.596+3468C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019324 | |||||||
| chr6:111019420 | G | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3564G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019420 | |||||||
| chr6:111019455 | T | C | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3599T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019455 | |||||||
| chr6:111019456 | T | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3600T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019456 | |||||||
| chr6:111019551 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0051 |
3 | NA18967.hp1 NA18982.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.596+3695A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019551 | |||||||
| chr6:111019590 | G | A | 200 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(197): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.596+3734G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019590 | |||||||
| chr6:111019629 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.596+3773C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019629 | |||||||
| chr6:111019754 | A | G | 99 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0036 others(96): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.596+3898A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019754 | |||||||
| chr6:111019755 | T | C | 1 | a0003c0003t0004g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.596+3899T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019755 | |||||||
| chr6:111019829 | A | C | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(92): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3973A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019829 | |||||||
| chr6:111019917 | C | CT | 3 | a0001c0001t0001g0291 a0001c0001t0001g0316 a0001c0001t0001g0323 |
3 | NA18949.hp1 NA18972.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.596+4065dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111019917 | ||||||
| chr6:111019917 | C | CTT | 79 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(76): Show |
80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.596+4064_596+4065d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111019917 | ||||||
| chr6:111019917 | C | CTTT | 16 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0105 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.596+4063_596+4065d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111019917 | ||||||
| chr6:111019917 | C | CTTTT | 4 | a0001c0001t0001g0030 a0001c0001t0004g0026 a0001c0001t0004g0028 others(1): Show |
4 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+4062_596+4065d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111019917 | ||||||
| chr6:111019922 | G | T | 102 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0042 others(99): Show |
103 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.596+4066G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019922 | |||||||
| chr6:111019975 | C | T | 12 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0003g0129 others(9): Show |
13 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.596+4119C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019975 | |||||||
| chr6:111020019 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.596+4163A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020019 | |||||||
| chr6:111020258 | C | T | 92 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0036 others(89): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.597-3925C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020258 | |||||||
| chr6:111020269 | A | G | 94 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0036 others(91): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-3914A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020269 | |||||||
| chr6:111020319 | G | A | 1 | a0001c0001t0004g0100 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.597-3864G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020319 | |||||||
| chr6:111020339 | G | A | 1 | a0001c0001t0006g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.597-3844G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020339 | |||||||
| chr6:111020384 | T | C | 7 | a0001c0001t0007g0020 a0001c0001t0007g0324 a0001c0001t0007g0325 others(4): Show |
8 | HG01952.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.597-3799T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020384 | |||||||
| chr6:111020451 | T | G | 1 | a0001c0001t0002g0238 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.597-3732T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020451 | |||||||
| chr6:111020466 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.597-3717C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020466 | |||||||
| chr6:111020491 | G | A | 75 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(72): Show |
75 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.597-3692G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020491 | |||||||
| chr6:111020704 | T | C | 305 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(302): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.597-3479T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020704 | |||||||
| chr6:111020859 | GA | G | 76 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0014 others(73): Show |
82 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.597-3316delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111020859 | ||||||
| chr6:111020876 | T | C | 9 | a0001c0001t0006g0012 a0001c0001t0006g0035 a0001c0001t0006g0108 others(6): Show |
10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.597-3307T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020876 | |||||||
| chr6:111020894 | C | T | 1 | a0003c0003t0003g0185 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.597-3289C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020894 | |||||||
| chr6:111020895 | G | A | 58 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0014 others(55): Show |
63 | HG00639.hp1 HG00642.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.597-3288G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020895 | |||||||
| chr6:111020966 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.597-3217G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020966 | |||||||
| chr6:111021095 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
38 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.597-3088G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021095 | |||||||
| chr6:111021113 | G | T | 4 | a0001c0005t0027g0043 a0002c0002t0010g0257 a0002c0002t0010g0258 others(1): Show |
4 | HG01433.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-3070G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021113 | |||||||
| chr6:111021215 | T | TAATA | 8 | a0001c0001t0006g0012 a0001c0001t0006g0035 a0001c0001t0006g0108 others(5): Show |
9 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.597-2967_597-2964d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111021215 | ||||||
| chr6:111021268 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.597-2915C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021268 | |||||||
| chr6:111021526 | A | G | 102 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(99): Show |
106 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.597-2657A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021526 | |||||||
| chr6:111021569 | C | T | 1 | a0001c0001t0004g0125 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.597-2614C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021569 | |||||||
| chr6:111021657 | C | T | 1 | a0001c0001t0002g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.597-2526C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021657 | |||||||
| chr6:111021819 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.597-2364A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021819 | |||||||
| chr6:111021903 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.597-2280A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021903 | |||||||
| chr6:111021987 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.597-2196A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021987 | |||||||
| chr6:111022191 | T | C | 79 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0014 others(76): Show |
85 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.597-1992T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022191 | |||||||
| chr6:111022225 | C | G | 17 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0092 others(14): Show |
19 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.597-1958C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022225 | |||||||
| chr6:111022252 | G | A | 1 | a0001c0001t0028g0310 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.597-1931G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022252 | |||||||
| chr6:111022319 | A | G | 9 | a0001c0001t0006g0012 a0001c0001t0006g0035 a0001c0001t0006g0108 others(6): Show |
10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.597-1864A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022319 | |||||||
| chr6:111022613 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.597-1570C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022613 | |||||||
| chr6:111022616 | T | TTG | 80 | a0001c0001t0002g0233 a0001c0001t0003g0010 a0001c0001t0003g0013 others(77): Show |
86 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.597-1564_597-1563d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111022616 | ||||||
| chr6:111022717 | G | T | 2 | a0001c0001t0012g0251 a0001c0001t0012g0265 |
2 | NA18987.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.597-1466G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022717 | |||||||
| chr6:111022907 | G | A | 3 | a0002c0002t0010g0257 a0002c0002t0010g0258 a0002c0002t0010g0259 |
3 | HG01433.hp2 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.597-1276G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022907 | |||||||
| chr6:111022967 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.597-1216C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022967 | |||||||
| chr6:111023160 | A | G | 1 | a0001c0001t0004g0028 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.597-1023A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023160 | |||||||
| chr6:111023323 | T | C | 1 | a0001c0001t0003g0151 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.597-860T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023323 | |||||||
| chr6:111023410 | G | A | 1 | a0001c0001t0006g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.597-773G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023410 | |||||||
| chr6:111023494 | G | A | 1 | a0001c0001t0015g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.597-689G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023494 | |||||||
| chr6:111023609 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.597-574G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023609 | |||||||
| chr6:111023643 | A | T | 2 | a0001c0001t0003g0128 a0001c0001t0003g0130 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.597-540A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023643 | |||||||
| chr6:111023644 | T | A | 2 | a0001c0001t0001g0030 a0001c0001t0003g0023 |
2 | HG01169.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597-539T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023644 | |||||||
| chr6:111023880 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.597-303C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023880 | |||||||
| chr6:111023982 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.597-201G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023982 | |||||||
| chr6:111023986 | C | CA | 107 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(104): Show |
112 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.597-184dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111023986 | ||||||
| chr6:111024049 | T | G | 80 | a0001c0001t0001g0042 a0001c0001t0003g0010 a0001c0001t0003g0013 others(77): Show |
86 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.597-134T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111024049 | |||||||
| chr6:111024139 | T | A | 1 | a0001c0001t0002g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.597-44T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111024139 | |||||||
| chr6:111024400 | T | C | 1 | a0001c0001t0001g0305 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.741+73T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024400 | |||||||
| chr6:111024479 | C | T | 100 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(97): Show |
104 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.741+152C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024479 | |||||||
| chr6:111024491 | A | G | 9 | a0001c0001t0006g0012 a0001c0001t0006g0035 a0001c0001t0006g0108 others(6): Show |
10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+164A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024491 | |||||||
| chr6:111024536 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.741+209A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024536 | |||||||
| chr6:111024611 | G | A | 1 | a0001c0001t0003g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.741+284G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024611 | |||||||
| chr6:111024652 | G | A | 1 | a0003c0003t0004g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.741+325G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024652 | |||||||
| chr6:111024674 | T | C | 9 | a0001c0001t0006g0012 a0001c0001t0006g0035 a0001c0001t0006g0108 others(6): Show |
10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+347T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024674 | |||||||
| chr6:111024704 | C | CA | 64 | a0001c0001t0001g0107 a0001c0001t0001g0303 a0001c0001t0001g0316 others(61): Show |
68 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.741+393dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 111024704 | ||||||
| chr6:111024704 | C | CAA | 9 | a0001c0001t0003g0134 a0001c0001t0003g0151 a0001c0001t0006g0012 others(6): Show |
10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+392_741+393dup others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 111024704 | ||||||
| chr6:111024757 | T | G | 1 | a0001c0001t0022g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.741+430T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024757 | |||||||
| chr6:111024760 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.741+433A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024760 | |||||||
| chr6:111024870 | T | C | 1 | a0001c0001t0003g0169 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.742-533T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024870 | |||||||
| chr6:111025143 | C | T | 9 | a0001c0001t0006g0012 a0001c0001t0006g0035 a0001c0001t0006g0108 others(6): Show |
10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.742-260C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111025143 | |||||||
| chr6:111025196 | T | C | 2 | a0001c0001t0013g0152 a0001c0001t0013g0186 |
2 | HG00741.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.742-207T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111025196 | |||||||
| chr6:111025238 | A | G | 1 | a0001c0001t0003g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.742-165A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111025238 |