Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5992 |
| ensemblid | ENSG00000111783.13 |
| hgncid | 9985 |
| symbol | RFX4 |
| name | regulatory factor X4 |
| refseq_nuc | NM_213594.3 |
| refseq_prot | NP_998759.1 |
| ensembl_nuc | ENST00000392842.6 |
| ensembl_prot | ENSP00000376585.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 106583004 |
| end | 106762803 |
| strand | + |
| ver | v1.2 |
| region | chr12:106583004-106762803 |
| region5000 | chr12:106578004-106767803 |
| regionname0 | RFX4_chr12_106583004_106762803 |
| regionname5000 | RFX4_chr12_106578004_106767803 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 735 | 292 | 84 | 63 | 95 | 12 | 36 | 73 | RFX4_chr12_106578004_106767803 | RFX4 | MHCGL others(730): Show |
chr12 | 106578004 | 106767803 |
| a0002 | 0/0 | 735 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | MHCGL others(730): Show |
chr12 | 106578004 | 106767803 |
| a0003 | 0/0 | 735 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | MHCGL others(730): Show |
chr12 | 106578004 | 106767803 |
| a0004 | 0/0 | 735 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | MHCGL others(730): Show |
chr12 | 106578004 | 106767803 |
| a0005 | 0/0 | 735 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | MHCGL others(730): Show |
chr12 | 106578004 | 106767803 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2205 | 167 | 41 | 37 | 61 | 6 | 20 | RFX4_chr12_106578004_106767803 | RFX4 | ATGCA others(2200): Show |
chr12 | 106578004 | 106767803 | ||
| a0001c0002 | 0/0 | 2205 | 107 | 28 | 24 | 34 | 6 | 15 | RFX4_chr12_106578004_106767803 | RFX4 | ATGCA others(2200): Show |
chr12 | 106578004 | 106767803 | ||
| a0001c0003 | 0/0 | 2205 | 14 | 11 | 2 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | ATGCA others(2200): Show |
chr12 | 106578004 | 106767803 | ||
| a0001c0004 | 0/0 | 2205 | 4 | 4 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | ATGCA others(2200): Show |
chr12 | 106578004 | 106767803 | ||
| a0002c0005 | 0/0 | 2205 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | ATGCA others(2200): Show |
chr12 | 106578004 | 106767803 | ||
| a0003c0006 | 0/0 | 2205 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | ATGCA others(2200): Show |
chr12 | 106578004 | 106767803 | ||
| a0004c0008 | 0/0 | 2205 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | ATGCA others(2200): Show |
chr12 | 106578004 | 106767803 | ||
| a0005c0007 | 0/0 | 2205 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | ATGCA others(2200): Show |
chr12 | 106578004 | 106767803 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3859 | 164 | 40 | 37 | 61 | 6 | 19 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0001c0001t0002 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0001c0001t0003 | 0/1 | 3859 | 1 | 0 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0001c0001t0004 | 0/0 | 3859 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0001c0002t0001 | 0/0 | 3859 | 105 | 26 | 24 | 34 | 6 | 15 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0001c0002t0005 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0001c0002t0006 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0001c0003t0001 | 0/0 | 3859 | 14 | 11 | 2 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0001c0004t0001 | 0/0 | 3859 | 4 | 4 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0002c0005t0001 | 0/0 | 3859 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0003c0006t0001 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0004c0008t0001 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| a0005c0007t0001 | 0/0 | 3859 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | GCAAA others(3854): Show |
chr12 | 106578004 | 106767803 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0279 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0003g0253 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0002t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0001c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0002c0005t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0003c0006t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0004c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| a0005c0007t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | GBR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0124 | EUR | GBR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0132 | EUR | GBR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | GBR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | CHS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | CHS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | CHS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | CHS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0143 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0074 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0136 | EUR | IBS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01943 | hp2 | a0002 | c0005 | t0001 | g0062 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | KHV | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | CDX | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0011 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0072 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02630 | hp2 | a0003 | c0006 | t0001 | g0116 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0228 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0073 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02717 | hp2 | a0004 | c0008 | t0001 | g0146 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0160 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0238 | AFR | MSL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | STU | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | STU | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0133 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | BEB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | STU | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0128 | SAS | STU | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | YRI | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | CHB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | YRI | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18948 | hp1 | a0005 | c0007 | t0001 | g0081 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | LWK | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19030 | hp2 | a0001 | c0002 | t0006 | g0147 | AFR | LWK | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ASW | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ASW | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0140 | EUR | TSI | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0130 | EUR | TSI | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0185 | EUR | TSI | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | GIH | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0188 | SAS | GIH | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02109 | hp2 | a0001 | c0002 | t0005 | g0061 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0101 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0110 | AFR | MSL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | USA | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | USA | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | USA | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0253 | REF | REF | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0279 | REF | REF | RFX4_chr12_106578004_106767803 | RFX4 | chr12 | 106578004 | 106767803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106711482 | C | T | 1 | a0003 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.964C>T | p.Arg322Trp | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/18 | 1281/3859 | 964/2208 | 322/735 | chr12 | 106711482 | |||
| chr12:106732203 | G | C | 1 | a0005 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.1425G>C | p.Glu475Asp | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/18 | 1742/3859 | 1425/2208 | 475/735 | chr12 | 106732203 | |||
| chr12:106747487 | G | A | 1 | a0002 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.1684G>A | p.Ala562Thr | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/18 | 2001/3859 | 1684/2208 | 562/735 | chr12 | 106747487 | |||
| chr12:106761353 | T | G | 1 | a0004 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2092T>G | p.Ser698Ala | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 18/18 | 2409/3859 | 2092/2208 | 698/735 | chr12 | 106761353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106696423 | T | C | 5 | a0001c0002 a0001c0003 a0001c0004 others(2): Show |
127 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(124): Show |
synonymous_variant | LOW | c.810T>C | p.Thr270Thr | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/18 | 1127/3859 | 810/2208 | 270/735 | chr12 | 106696423 | |||
| chr12:106719991 | G | A | 3 | a0001c0003 a0002c0005 a0003c0006 |
16 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(13): Show |
synonymous_variant | LOW | c.1170G>A | p.Glu390Glu | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 12/18 | 1487/3859 | 1170/2208 | 390/735 | chr12 | 106719991 | |||
| chr12:106720770 | G | A | 1 | a0001c0004 | 4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.1245G>A | p.Lys415Lys | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/18 | 1562/3859 | 1245/2208 | 415/735 | chr12 | 106720770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106583201 | T | G | 1 | a0001c0001t0002 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/18 | 120 | chr12 | 106583201 | ||||||
| chr12:106761885 | G | T | 1 | a0001c0002t0006 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*416G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 18/18 | 416 | chr12 | 106761885 | ||||||
| chr12:106762358 | C | G | 1 | a0001c0002t0005 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*889C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 18/18 | 889 | chr12 | 106762358 | ||||||
| chr12:106762718 | T | C | 1 | a0001c0001t0004 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1249T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 18/18 | 1249 | chr12 | 106762718 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106583648 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+285G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106583648 | |||||||
| chr12:106584042 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG01258.hp2 HG01517.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+679G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106584042 | |||||||
| chr12:106584119 | A | AG | 274 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(271): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.43+757dupG | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106584119 | ||||||
| chr12:106584292 | G | C | 1 | a0001c0001t0001g0008 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.43+929G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106584292 | |||||||
| chr12:106584533 | G | A | 55 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(52): Show |
55 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.43+1170G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106584533 | |||||||
| chr12:106584718 | C | T | 4 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 others(1): Show |
4 | HG02135.hp2 NA18951.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+1355C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106584718 | |||||||
| chr12:106584787 | TGATTCCT others(3): Show |
T | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+1426_43+1435del others(10): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106584787 | ||||||
| chr12:106584846 | G | A | 1 | a0001c0003t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.43+1483G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106584846 | |||||||
| chr12:106584884 | T | C | 1 | a0001c0002t0001g0272 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.43+1521T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106584884 | |||||||
| chr12:106584932 | T | C | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+1569T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106584932 | |||||||
| chr12:106585219 | G | A | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+1856G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106585219 | |||||||
| chr12:106585261 | G | A | 51 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0076 others(48): Show |
51 | HG00408.hp1 HG00438.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.43+1898G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106585261 | |||||||
| chr12:106585349 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG01943.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.43+1986G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106585349 | |||||||
| chr12:106585409 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.43+2046C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106585409 | |||||||
| chr12:106585413 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.43+2050G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106585413 | |||||||
| chr12:106585639 | T | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+2276T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106585639 | |||||||
| chr12:106585705 | G | T | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.43+2342G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106585705 | |||||||
| chr12:106585860 | G | T | 3 | a0001c0002t0001g0137 a0001c0002t0001g0138 a0001c0002t0001g0139 |
3 | HG01099.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.43+2497G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106585860 | |||||||
| chr12:106585970 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.43+2607T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106585970 | |||||||
| chr12:106586017 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.43+2654G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586017 | |||||||
| chr12:106586055 | C | A | 6 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(3): Show |
6 | HG02280.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+2692C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586055 | |||||||
| chr12:106586261 | C | G | 4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | NA18990.hp1 NA19005.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+2898C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586261 | |||||||
| chr12:106586262 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.43+2899G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586262 | |||||||
| chr12:106586273 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.43+2910C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586273 | |||||||
| chr12:106586476 | A | G | 170 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0076 others(167): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.43+3113A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586476 | |||||||
| chr12:106586484 | G | A | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+3121G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586484 | |||||||
| chr12:106586612 | G | A | 3 | a0001c0002t0001g0142 a0001c0003t0001g0141 a0001c0003t0001g0143 |
3 | HG01109.hp2 HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.43+3249G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586612 | |||||||
| chr12:106586839 | C | T | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+3476C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586839 | |||||||
| chr12:106586980 | T | C | 56 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(53): Show |
56 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.43+3617T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586980 | |||||||
| chr12:106586982 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0002t0001g0002 |
3 | HG02027.hp1 HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.43+3619C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106586982 | |||||||
| chr12:106587085 | A | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(9): Show |
12 | HG01109.hp2 HG01516.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.43+3722A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106587085 | |||||||
| chr12:106587100 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+3737C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106587100 | |||||||
| chr12:106587306 | G | A | 56 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(53): Show |
56 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.43+3943G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106587306 | |||||||
| chr12:106587399 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.43+4036C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106587399 | |||||||
| chr12:106587536 | T | G | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+4173T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106587536 | |||||||
| chr12:106587537 | C | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+4174C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106587537 | |||||||
| chr12:106587538 | C | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+4175C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106587538 | |||||||
| chr12:106587735 | C | T | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.43+4372C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106587735 | |||||||
| chr12:106588032 | G | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.43+4669G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588032 | |||||||
| chr12:106588193 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+4830A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588193 | |||||||
| chr12:106588207 | G | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.43+4844G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588207 | |||||||
| chr12:106588389 | A | G | 3 | a0001c0002t0001g0002 a0001c0002t0001g0070 a0001c0002t0001g0071 |
3 | HG02027.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+5026A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588389 | |||||||
| chr12:106588555 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.43+5192C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588555 | |||||||
| chr12:106588679 | A | T | 2 | a0001c0001t0001g0259 a0001c0002t0001g0258 |
2 | NA18954.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.43+5316A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588679 | |||||||
| chr12:106588735 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+5372G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588735 | |||||||
| chr12:106588736 | C | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+5373C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588736 | |||||||
| chr12:106588758 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.43+5395T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588758 | |||||||
| chr12:106588827 | C | T | 9 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(6): Show |
9 | HG01167.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+5464C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588827 | |||||||
| chr12:106588871 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | NA18982.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.43+5508A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588871 | |||||||
| chr12:106588931 | G | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+5568G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106588931 | |||||||
| chr12:106589225 | T | A | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.43+5862T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106589225 | |||||||
| chr12:106589332 | G | A | 42 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(39): Show |
42 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.43+5969G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106589332 | |||||||
| chr12:106589511 | C | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(1): Show |
4 | HG02922.hp1 HG03139.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+6148C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106589511 | |||||||
| chr12:106589733 | G | A | 1 | a0001c0002t0001g0021 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.43+6370G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106589733 | |||||||
| chr12:106589742 | A | G | 3 | a0001c0002t0001g0002 a0001c0002t0001g0070 a0001c0002t0001g0071 |
3 | HG02027.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+6379A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106589742 | |||||||
| chr12:106590010 | C | A | 4 | a0001c0002t0001g0155 a0001c0002t0001g0272 a0001c0002t0001g0273 others(1): Show |
4 | HG02135.hp2 NA18747.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+6647C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590010 | |||||||
| chr12:106590056 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.43+6693A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590056 | |||||||
| chr12:106590078 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.43+6715A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590078 | |||||||
| chr12:106590298 | C | T | 5 | a0001c0002t0001g0142 a0001c0003t0001g0141 a0001c0003t0001g0143 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+6935C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590298 | |||||||
| chr12:106590299 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+6936G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590299 | |||||||
| chr12:106590344 | A | G | 2 | a0001c0002t0001g0056 a0001c0002t0001g0057 |
2 | HG01168.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.43+6981A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590344 | |||||||
| chr12:106590570 | T | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0070 a0001c0002t0001g0071 |
3 | HG02027.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+7207T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590570 | |||||||
| chr12:106590572 | C | A | 8 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(5): Show |
8 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+7209C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590572 | |||||||
| chr12:106590601 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.43+7238C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590601 | |||||||
| chr12:106590671 | T | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0070 a0001c0002t0001g0071 |
3 | HG02027.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+7308T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590671 | |||||||
| chr12:106590732 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.43+7369G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590732 | |||||||
| chr12:106590775 | A | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+7412A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590775 | |||||||
| chr12:106590811 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+7448G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590811 | |||||||
| chr12:106590894 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+7531C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590894 | |||||||
| chr12:106590954 | A | C | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.43+7591A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106590954 | |||||||
| chr12:106591259 | TC | T | 43 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
43 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.43+7899delC | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106591259 | ||||||
| chr12:106591261 | C | CT | 31 | a0001c0001t0001g0008 a0001c0001t0001g0112 a0001c0001t0001g0113 others(28): Show |
31 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.43+7898_43+7899ins others(1): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591261 | |||||||
| chr12:106591261 | C | CTT | 20 | a0001c0001t0001g0001 a0001c0001t0001g0123 a0001c0001t0001g0131 others(17): Show |
21 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.43+7898_43+7899ins others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591261 | |||||||
| chr12:106591261 | C | CTTT | 3 | a0001c0001t0001g0118 a0001c0002t0001g0133 a0001c0002t0001g0134 |
3 | HG03831.hp1 HG04184.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.43+7898_43+7899ins others(3): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591261 | |||||||
| chr12:106591261 | CCT | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02257.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+7899_43+7900del others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591261 | |||||||
| chr12:106591261 | CCTT | C | 3 | a0001c0001t0001g0150 a0001c0002t0001g0070 a0001c0002t0001g0071 |
3 | HG02723.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+7899_43+7901del others(3): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591261 | |||||||
| chr12:106591261 | CCTTTTTT | C | 6 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(3): Show |
6 | HG02280.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+7899_43+7905del others(7): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591261 | |||||||
| chr12:106591262 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.43+7899C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591262 | |||||||
| chr12:106591275 | T | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+7912T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591275 | |||||||
| chr12:106591281 | T | TC | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+7918_43+7919ins others(1): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591281 | |||||||
| chr12:106591310 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.43+7947C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591310 | |||||||
| chr12:106591416 | C | T | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43+8053C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591416 | |||||||
| chr12:106591545 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.43+8182C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591545 | |||||||
| chr12:106591655 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.43+8292G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591655 | |||||||
| chr12:106591967 | A | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+8604A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106591967 | |||||||
| chr12:106592037 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.43+8674A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592037 | |||||||
| chr12:106592044 | T | A | 1 | a0001c0002t0001g0237 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.43+8681T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592044 | |||||||
| chr12:106592180 | T | A | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.43+8817T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592180 | |||||||
| chr12:106592206 | G | GA | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(4): Show |
7 | HG01361.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+8853dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106592206 | ||||||
| chr12:106592206 | GA | G | 182 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0076 others(179): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.43+8853delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106592206 | ||||||
| chr12:106592357 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.43+8994A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592357 | |||||||
| chr12:106592462 | C | T | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02257.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+9099C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592462 | |||||||
| chr12:106592512 | T | C | 1 | a0001c0002t0001g0155 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.43+9149T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592512 | |||||||
| chr12:106592618 | C | T | 1 | a0001c0002t0001g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.43+9255C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592618 | |||||||
| chr12:106592815 | C | T | 228 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0022 others(225): Show |
228 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.43+9452C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592815 | |||||||
| chr12:106592829 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0165 |
3 | HG00738.hp2 HG01099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.43+9466G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592829 | |||||||
| chr12:106592870 | T | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG00621.hp2 HG03492.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.43+9507T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592870 | |||||||
| chr12:106592904 | C | T | 168 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0076 others(165): Show |
168 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.43+9541C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592904 | |||||||
| chr12:106592905 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+9542G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592905 | |||||||
| chr12:106592911 | G | T | 5 | a0001c0002t0001g0142 a0001c0003t0001g0141 a0001c0003t0001g0143 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+9548G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106592911 | |||||||
| chr12:106593128 | T | C | 230 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0022 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.43+9765T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106593128 | |||||||
| chr12:106593258 | G | A | 1 | a0001c0003t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.43+9895G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106593258 | |||||||
| chr12:106593325 | G | A | 221 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0022 others(218): Show |
221 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.43+9962G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106593325 | |||||||
| chr12:106593458 | G | C | 230 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0022 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.43+10095G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106593458 | |||||||
| chr12:106593541 | A | C | 1 | a0001c0001t0001g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43+10178A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106593541 | |||||||
| chr12:106593716 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.43+10353A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106593716 | |||||||
| chr12:106593751 | C | T | 1 | a0001c0002t0001g0235 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.43+10388C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106593751 | |||||||
| chr12:106593843 | T | C | 8 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
8 | NA18948.hp1 NA18964.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+10480T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106593843 | |||||||
| chr12:106594288 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43+10925T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106594288 | |||||||
| chr12:106594332 | G | C | 230 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0022 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.43+10969G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106594332 | |||||||
| chr12:106594802 | T | TA | 166 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0076 others(163): Show |
166 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.43+11453dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106594802 | ||||||
| chr12:106594817 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.43+11454G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106594817 | |||||||
| chr12:106594839 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.43+11476A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106594839 | |||||||
| chr12:106594909 | C | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0136 others(6): Show |
9 | HG01109.hp2 HG01516.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+11546C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106594909 | |||||||
| chr12:106595012 | T | A | 1 | a0001c0002t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.43+11649T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595012 | |||||||
| chr12:106595090 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.43+11727C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595090 | |||||||
| chr12:106595144 | T | C | 230 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0022 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.43+11781T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595144 | |||||||
| chr12:106595262 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.43+11899T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595262 | |||||||
| chr12:106595266 | C | T | 5 | a0001c0002t0001g0142 a0001c0003t0001g0141 a0001c0003t0001g0143 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+11903C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595266 | |||||||
| chr12:106595327 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+11964C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595327 | |||||||
| chr12:106595353 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.43+11990G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595353 | |||||||
| chr12:106595393 | A | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+12030A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595393 | |||||||
| chr12:106595549 | A | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+12186A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595549 | |||||||
| chr12:106595660 | A | G | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+12297A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595660 | |||||||
| chr12:106595793 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0170 a0001c0002t0001g0239 |
3 | HG02056.hp1 NA18943.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.43+12430G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595793 | |||||||
| chr12:106595835 | A | G | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.43+12472A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595835 | |||||||
| chr12:106595847 | T | C | 229 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0022 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.43+12484T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106595847 | |||||||
| chr12:106596041 | C | A | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43+12678C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106596041 | |||||||
| chr12:106596092 | C | A | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.44-12705C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106596092 | |||||||
| chr12:106596129 | G | A | 5 | a0001c0002t0001g0142 a0001c0003t0001g0141 a0001c0003t0001g0143 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-12668G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106596129 | |||||||
| chr12:106596137 | A | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(221): Show |
224 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.44-12660A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106596137 | |||||||
| chr12:106596208 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.44-12589A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106596208 | |||||||
| chr12:106596395 | C | A | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0236 others(10): Show |
13 | HG01109.hp2 HG01175.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-12402C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106596395 | |||||||
| chr12:106596476 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.44-12321G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106596476 | |||||||
| chr12:106596605 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.44-12192C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106596605 | |||||||
| chr12:106596741 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.44-12056G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106596741 | |||||||
| chr12:106597063 | G | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(26): Show |
29 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.44-11734G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597063 | |||||||
| chr12:106597237 | A | C | 1 | a0001c0002t0001g0229 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.44-11560A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597237 | |||||||
| chr12:106597260 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.44-11537A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597260 | |||||||
| chr12:106597569 | T | G | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.44-11228T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597569 | |||||||
| chr12:106597665 | G | A | 1 | a0001c0002t0001g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.44-11132G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597665 | |||||||
| chr12:106597734 | C | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(27): Show |
30 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.44-11063C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597734 | |||||||
| chr12:106597742 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.44-11055C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597742 | |||||||
| chr12:106597767 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(94): Show |
98 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.44-11030A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597767 | |||||||
| chr12:106597828 | C | T | 20 | a0001c0001t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(17): Show |
20 | HG01109.hp2 HG01243.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.44-10969C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597828 | |||||||
| chr12:106597854 | C | T | 1 | a0001c0003t0001g0074 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.44-10943C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597854 | |||||||
| chr12:106597916 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.44-10881G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106597916 | |||||||
| chr12:106598184 | C | T | 4 | a0001c0001t0001g0156 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-10613C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106598184 | |||||||
| chr12:106598187 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-10610G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106598187 | |||||||
| chr12:106598233 | C | T | 1 | a0001c0003t0001g0145 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.44-10564C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106598233 | |||||||
| chr12:106598418 | GTTACAGT others(29): Show |
G | 1 | a0001c0002t0001g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.44-10376_44-10341d others(38): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106598418 | ||||||
| chr12:106598496 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-10301C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106598496 | |||||||
| chr12:106598497 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(27): Show |
30 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.44-10300C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106598497 | |||||||
| chr12:106598694 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.44-10103T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106598694 | |||||||
| chr12:106598727 | GA | G | 8 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(5): Show |
8 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-10069delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106598727 | |||||||
| chr12:106598926 | C | T | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.44-9871C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106598926 | |||||||
| chr12:106598962 | T | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-9835T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106598962 | |||||||
| chr12:106599130 | C | T | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-9667C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106599130 | |||||||
| chr12:106599184 | GT | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0118 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.44-9600delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106599184 | ||||||
| chr12:106599284 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.44-9513G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106599284 | |||||||
| chr12:106599314 | A | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0118 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.44-9483A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106599314 | |||||||
| chr12:106599471 | G | GTGA | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG01884.hp1 NA19004.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-9289_44-9287dup others(3): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106599471 | ||||||
| chr12:106599471 | G | GTGATGA | 8 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(5): Show |
8 | HG02572.hp2 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-9292_44-9287dup others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106599471 | ||||||
| chr12:106599471 | GTGA | G | 4 | a0001c0001t0001g0164 a0001c0001t0002g0173 a0001c0002t0001g0068 others(1): Show |
4 | HG03225.hp1 HG03834.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-9289_44-9287del others(3): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106599471 | ||||||
| chr12:106599471 | GTGATGA | G | 8 | a0001c0002t0001g0049 a0001c0002t0001g0063 a0001c0002t0001g0064 others(5): Show |
8 | HG00609.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-9292_44-9287del others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106599471 | ||||||
| chr12:106599471 | GTGATGAT others(2): Show |
G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(67): Show |
71 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.44-9295_44-9287del others(9): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106599471 | ||||||
| chr12:106599471 | GTGATGAT others(5): Show |
G | 21 | a0001c0001t0001g0131 a0001c0001t0001g0150 a0001c0001t0001g0151 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.44-9298_44-9287del others(12): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106599471 | ||||||
| chr12:106599731 | C | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.44-9066C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106599731 | |||||||
| chr12:106600160 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.44-8637C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106600160 | |||||||
| chr12:106600163 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.44-8634G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106600163 | |||||||
| chr12:106600344 | C | T | 31 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(28): Show |
31 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.44-8453C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106600344 | |||||||
| chr12:106600401 | G | A | 18 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0002t0001g0013 others(15): Show |
18 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-8396G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106600401 | |||||||
| chr12:106600749 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.44-8048G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106600749 | |||||||
| chr12:106600782 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.44-8015C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106600782 | |||||||
| chr12:106600853 | C | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | NA18982.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.44-7944C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106600853 | |||||||
| chr12:106601023 | C | T | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44-7774C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601023 | |||||||
| chr12:106601026 | T | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(97): Show |
101 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.44-7771T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601026 | |||||||
| chr12:106601187 | T | C | 39 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(36): Show |
39 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.44-7610T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601187 | |||||||
| chr12:106601321 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.44-7476C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601321 | |||||||
| chr12:106601331 | C | G | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-7466C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601331 | |||||||
| chr12:106601358 | G | C | 39 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(36): Show |
39 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.44-7439G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601358 | |||||||
| chr12:106601491 | G | C | 110 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0030 others(107): Show |
110 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.44-7306G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601491 | |||||||
| chr12:106601650 | G | A | 8 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(5): Show |
8 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-7147G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601650 | |||||||
| chr12:106601710 | G | A | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-7087G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601710 | |||||||
| chr12:106601800 | G | A | 1 | a0001c0002t0001g0032 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.44-6997G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106601800 | |||||||
| chr12:106602204 | G | A | 2 | a0001c0002t0001g0002 a0001c0002t0001g0049 |
2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.44-6593G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106602204 | |||||||
| chr12:106602478 | A | G | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02602.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.44-6319A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106602478 | |||||||
| chr12:106602480 | G | T | 5 | a0001c0001t0001g0161 a0001c0002t0001g0031 a0001c0002t0001g0162 others(2): Show |
5 | NA18954.hp2 NA19010.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-6317G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106602480 | |||||||
| chr12:106602484 | GGATTTGA others(10): Show |
G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.44-6305_44-6289del others(17): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106602484 | ||||||
| chr12:106602532 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.44-6265A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106602532 | |||||||
| chr12:106602873 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.44-5924A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106602873 | |||||||
| chr12:106603043 | T | A | 1 | a0001c0002t0001g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.44-5754T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603043 | |||||||
| chr12:106603295 | G | A | 1 | a0001c0002t0001g0225 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.44-5502G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603295 | |||||||
| chr12:106603412 | C | A | 2 | a0001c0002t0001g0013 a0001c0002t0001g0014 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.44-5385C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603412 | |||||||
| chr12:106603463 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0083 |
2 | HG00609.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.44-5334C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603463 | |||||||
| chr12:106603549 | C | T | 1 | a0001c0002t0001g0225 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.44-5248C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603549 | |||||||
| chr12:106603568 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.44-5229G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603568 | |||||||
| chr12:106603673 | T | C | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.44-5124T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603673 | |||||||
| chr12:106603711 | T | C | 6 | a0001c0002t0001g0155 a0001c0002t0001g0174 a0001c0002t0001g0229 others(3): Show |
6 | HG02135.hp2 NA18747.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-5086T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603711 | |||||||
| chr12:106603929 | A | T | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.44-4868A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603929 | |||||||
| chr12:106603967 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-4830C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603967 | |||||||
| chr12:106603968 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.44-4829G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106603968 | |||||||
| chr12:106604115 | C | CT | 19 | a0001c0001t0001g0105 a0001c0001t0001g0154 a0001c0001t0001g0216 others(16): Show |
19 | HG00099.hp2 HG00609.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.44-4660dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106604115 | ||||||
| chr12:106604115 | C | CTT | 27 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(24): Show |
28 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.44-4661_44-4660dup others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106604115 | ||||||
| chr12:106604115 | CT | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0148 others(25): Show |
28 | HG01109.hp2 HG01175.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.44-4660delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106604115 | ||||||
| chr12:106604164 | A | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(22): Show |
26 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.44-4633A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106604164 | |||||||
| chr12:106604265 | C | T | 1 | a0001c0002t0001g0225 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.44-4532C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106604265 | |||||||
| chr12:106604310 | C | T | 2 | a0001c0002t0001g0215 a0001c0002t0001g0234 |
2 | NA18942.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.44-4487C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106604310 | |||||||
| chr12:106604350 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.44-4447G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106604350 | |||||||
| chr12:106604356 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.44-4441C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106604356 | |||||||
| chr12:106604506 | G | A | 7 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0003t0001g0060 others(4): Show |
7 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-4291G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106604506 | |||||||
| chr12:106604544 | T | TA | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0118 others(50): Show |
54 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.44-4241dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106604544 | ||||||
| chr12:106605127 | C | A | 1 | a0001c0002t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.44-3670C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106605127 | |||||||
| chr12:106605240 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.44-3557T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106605240 | |||||||
| chr12:106605293 | A | G | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.44-3504A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106605293 | |||||||
| chr12:106605438 | C | T | 7 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0002t0001g0238 others(4): Show |
7 | HG01109.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-3359C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106605438 | |||||||
| chr12:106605457 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.44-3340C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106605457 | |||||||
| chr12:106605616 | G | A | 2 | a0001c0003t0001g0072 a0001c0003t0001g0074 |
2 | HG01175.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.44-3181G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106605616 | |||||||
| chr12:106605718 | G | A | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44-3079G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106605718 | |||||||
| chr12:106605790 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(6): Show |
9 | HG01109.hp2 HG01943.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-3007G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106605790 | |||||||
| chr12:106606013 | C | A | 1 | a0001c0001t0001g0175 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.44-2784C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606013 | |||||||
| chr12:106606104 | A | G | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.44-2693A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606104 | |||||||
| chr12:106606105 | G | A | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.44-2692G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606105 | |||||||
| chr12:106606118 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.44-2679G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606118 | |||||||
| chr12:106606204 | A | C | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.44-2593A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606204 | |||||||
| chr12:106606248 | G | A | 2 | a0001c0002t0001g0176 a0001c0002t0001g0240 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.44-2549G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606248 | |||||||
| chr12:106606375 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-2422G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606375 | |||||||
| chr12:106606521 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.44-2276C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606521 | |||||||
| chr12:106606824 | C | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(22): Show |
25 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(22): Show |
intron_variant | MODIFIER | c.44-1973C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606824 | |||||||
| chr12:106606889 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.44-1908G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106606889 | |||||||
| chr12:106607063 | G | A | 11 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(8): Show |
11 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.44-1734G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106607063 | |||||||
| chr12:106607130 | A | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(25): Show |
28 | HG00609.hp1 HG01109.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.44-1667A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106607130 | |||||||
| chr12:106607135 | C | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.44-1662C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106607135 | |||||||
| chr12:106607258 | T | C | 1 | a0004c0008t0001g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.44-1539T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106607258 | |||||||
| chr12:106607312 | C | G | 7 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0003t0001g0060 others(4): Show |
7 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-1485C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106607312 | |||||||
| chr12:106607508 | G | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0112 |
3 | NA18966.hp1 NA18978.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.44-1289G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106607508 | |||||||
| chr12:106607509 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.44-1288G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106607509 | |||||||
| chr12:106607577 | TG | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(23): Show |
26 | HG00609.hp1 HG01175.hp1 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.44-1212delG | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106607577 | ||||||
| chr12:106607762 | G | GATGA | 4 | a0001c0001t0001g0024 a0001c0002t0001g0002 a0001c0002t0001g0049 others(1): Show |
4 | HG00609.hp1 HG01361.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-1011_44-1008dup others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106607762 | ||||||
| chr12:106607762 | GATGA | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0035 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.44-1011_44-1008del others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106607762 | ||||||
| chr12:106607787 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0249 |
2 | NA18966.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.44-1010A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106607787 | |||||||
| chr12:106607827 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0249 |
2 | NA18966.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.44-970A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106607827 | |||||||
| chr12:106608113 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.44-684C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106608113 | |||||||
| chr12:106608451 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.44-346C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106608451 | |||||||
| chr12:106608599 | T | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(25): Show |
28 | HG00609.hp1 HG01109.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.44-198T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | chr12 | 106608599 | |||||||
| chr12:106608780 | CT | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(84): Show |
splice_region_variant&intron_variant | LOW | c.44-3delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106608780 | ||||||
| chr12:106608780 | CTT | C | 6 | a0001c0002t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0109 others(3): Show |
6 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.44-4_44-3delTT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr12 | 106608780 | ||||||
| chr12:106608931 | T | C | 18 | a0001c0001t0001g0131 a0001c0002t0001g0119 a0001c0002t0001g0120 others(15): Show |
18 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.130+48T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106608931 | |||||||
| chr12:106609045 | A | G | 1 | a0001c0003t0001g0110 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+162A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106609045 | |||||||
| chr12:106609047 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(25): Show |
28 | HG00609.hp1 HG01109.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.130+164G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106609047 | |||||||
| chr12:106609523 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+640T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106609523 | |||||||
| chr12:106609710 | G | A | 11 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(8): Show |
11 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+827G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106609710 | |||||||
| chr12:106609742 | GT | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(25): Show |
28 | HG00609.hp1 HG01109.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.130+869delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106609742 | ||||||
| chr12:106609750 | T | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.130+867T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106609750 | |||||||
| chr12:106609784 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(25): Show |
28 | HG00609.hp1 HG01109.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.130+901T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106609784 | |||||||
| chr12:106610144 | A | C | 15 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(12): Show |
15 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+1261A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610144 | |||||||
| chr12:106610145 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+1262G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610145 | |||||||
| chr12:106610149 | A | C | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130+1266A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610149 | |||||||
| chr12:106610202 | C | T | 3 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 |
3 | HG02135.hp2 NA18951.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.130+1319C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610202 | |||||||
| chr12:106610231 | C | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0035 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.130+1348C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610231 | |||||||
| chr12:106610237 | CA | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(74): Show |
78 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.130+1375delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106610237 | ||||||
| chr12:106610237 | CAA | C | 11 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+1374_130+1375d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106610237 | ||||||
| chr12:106610348 | A | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(28): Show |
31 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.130+1465A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610348 | |||||||
| chr12:106610607 | T | A | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.130+1724T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610607 | |||||||
| chr12:106610635 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.130+1752G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610635 | |||||||
| chr12:106610662 | G | A | 1 | a0001c0003t0001g0074 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.130+1779G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610662 | |||||||
| chr12:106610738 | G | C | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+1855G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610738 | |||||||
| chr12:106610945 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0035 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.130+2062A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106610945 | |||||||
| chr12:106611402 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.130+2519T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106611402 | |||||||
| chr12:106611409 | C | CT | 43 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0076 others(40): Show |
43 | HG00408.hp1 HG00438.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.130+2536dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106611409 | ||||||
| chr12:106611507 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+2624G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106611507 | |||||||
| chr12:106611515 | C | CT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.130+2645dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106611515 | ||||||
| chr12:106611597 | G | A | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.130+2714G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106611597 | |||||||
| chr12:106611668 | G | A | 7 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0003t0001g0060 others(4): Show |
7 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+2785G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106611668 | |||||||
| chr12:106611854 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.130+2971A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106611854 | |||||||
| chr12:106612198 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.130+3315A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106612198 | |||||||
| chr12:106612452 | T | A | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.130+3569T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106612452 | |||||||
| chr12:106612635 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.130+3752C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106612635 | |||||||
| chr12:106612772 | A | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.130+3889A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106612772 | |||||||
| chr12:106612802 | C | A | 42 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0167 others(39): Show |
42 | HG00438.hp1 HG00621.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.130+3919C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106612802 | |||||||
| chr12:106613338 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130+4455T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106613338 | |||||||
| chr12:106613366 | AT | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0035 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.130+4498delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106613366 | ||||||
| chr12:106613387 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(25): Show |
28 | HG00609.hp1 HG01109.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.130+4504C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106613387 | |||||||
| chr12:106613391 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.130+4508C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106613391 | |||||||
| chr12:106613482 | C | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01361.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+4599C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106613482 | |||||||
| chr12:106613508 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130+4625G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106613508 | |||||||
| chr12:106613516 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.130+4633C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106613516 | |||||||
| chr12:106613832 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.130+4949T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106613832 | |||||||
| chr12:106614057 | G | A | 1 | a0001c0002t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.130+5174G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614057 | |||||||
| chr12:106614061 | A | G | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+5178A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614061 | |||||||
| chr12:106614128 | A | C | 1 | a0001c0002t0001g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.130+5245A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614128 | |||||||
| chr12:106614184 | G | A | 12 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(9): Show |
12 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+5301G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614184 | |||||||
| chr12:106614266 | T | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.130+5383T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614266 | |||||||
| chr12:106614381 | G | C | 1 | a0001c0001t0001g0178 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.130+5498G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614381 | |||||||
| chr12:106614459 | C | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.130+5576C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614459 | |||||||
| chr12:106614477 | C | CTG | 59 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0076 others(56): Show |
59 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.130+5636_130+5637d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | C | CTGTG | 54 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(51): Show |
54 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.130+5634_130+5637d others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | C | CTGTGTG | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
71 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.130+5632_130+5637d others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | C | CTGTGTGT others(1): Show |
10 | a0001c0001t0001g0024 a0001c0001t0001g0088 a0001c0001t0001g0107 others(7): Show |
10 | HG01069.hp1 HG01361.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+5630_130+5637d others(10): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | C | CTGTGTGT others(3): Show |
9 | a0001c0001t0001g0080 a0001c0001t0001g0158 a0001c0001t0001g0213 others(6): Show |
9 | HG01516.hp1 HG01517.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+5628_130+5637d others(12): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0236 a0001c0001t0001g0271 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.130+5624_130+5637d others(16): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | CTGTG | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.130+5634_130+5637d others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | CTGTGTG | C | 4 | a0001c0002t0001g0056 a0001c0002t0001g0070 a0001c0002t0001g0071 others(1): Show |
4 | HG01168.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+5632_130+5637d others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | CTGTGTGT others(3): Show |
C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0002t0001g0068 |
3 | HG02486.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.130+5628_130+5637d others(12): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | CTGTGTGT others(7): Show |
C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+5624_130+5637d others(16): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614477 | CTGTGTGT others(9): Show |
C | 14 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(11): Show |
14 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+5622_130+5637d others(18): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106614477 | ||||||
| chr12:106614520 | T | TGTGTG | 9 | a0001c0001t0001g0113 a0001c0001t0001g0154 a0001c0001t0001g0161 others(6): Show |
9 | HG00735.hp1 HG02698.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+5637_130+5638i others(7): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614520 | |||||||
| chr12:106614521 | T | G | 1 | a0001c0002t0001g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+5638T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614521 | |||||||
| chr12:106614539 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.130+5656C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614539 | |||||||
| chr12:106614581 | T | G | 14 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(11): Show |
14 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+5698T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614581 | |||||||
| chr12:106614594 | C | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0103 a0001c0001t0001g0105 others(1): Show |
4 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+5711C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614594 | |||||||
| chr12:106614759 | T | G | 3 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 |
3 | HG02280.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.130+5876T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614759 | |||||||
| chr12:106614809 | G | A | 7 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0003t0001g0060 others(4): Show |
7 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+5926G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614809 | |||||||
| chr12:106614854 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.130+5971G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614854 | |||||||
| chr12:106614930 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.130+6047C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614930 | |||||||
| chr12:106614966 | C | T | 15 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(12): Show |
15 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+6083C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106614966 | |||||||
| chr12:106615093 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0002t0001g0068 |
3 | HG02486.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.130+6210C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615093 | |||||||
| chr12:106615095 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(22): Show |
25 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+6212T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615095 | |||||||
| chr12:106615180 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02895.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.130+6297G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615180 | |||||||
| chr12:106615203 | T | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.130+6320T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615203 | |||||||
| chr12:106615269 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.130+6386A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615269 | |||||||
| chr12:106615289 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.130+6406A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615289 | |||||||
| chr12:106615310 | G | C | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130+6427G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615310 | |||||||
| chr12:106615889 | T | A | 12 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(9): Show |
12 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+7006T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615889 | |||||||
| chr12:106615891 | A | G | 2 | a0001c0002t0001g0176 a0001c0002t0001g0240 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.130+7008A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615891 | |||||||
| chr12:106615902 | T | G | 1 | a0001c0002t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.130+7019T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615902 | |||||||
| chr12:106615950 | A | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.130+7067A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106615950 | |||||||
| chr12:106616138 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.130+7255A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106616138 | |||||||
| chr12:106616272 | G | A | 1 | a0001c0003t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.130+7389G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106616272 | |||||||
| chr12:106616606 | G | A | 5 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0001g0289 others(2): Show |
5 | HG02602.hp1 NA18939.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+7723G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106616606 | |||||||
| chr12:106616860 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.130+7977A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106616860 | |||||||
| chr12:106616935 | A | AT | 11 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0148 others(8): Show |
11 | HG00621.hp2 HG01109.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+8065dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106616935 | ||||||
| chr12:106617164 | T | C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.130+8281T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617164 | |||||||
| chr12:106617188 | A | G | 1 | a0001c0002t0001g0185 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.130+8305A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617188 | |||||||
| chr12:106617192 | G | A | 3 | a0001c0002t0001g0165 a0001c0002t0001g0180 a0001c0002t0001g0185 |
3 | HG01256.hp2 HG03704.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.130+8309G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617192 | |||||||
| chr12:106617192 | G | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.130+8309G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617192 | |||||||
| chr12:106617232 | T | G | 1 | a0001c0001t0001g0265 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.130+8349T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617232 | |||||||
| chr12:106617268 | T | G | 32 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(29): Show |
32 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.130+8385T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617268 | |||||||
| chr12:106617469 | T | C | 1 | a0001c0001t0001g0287 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.130+8586T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617469 | |||||||
| chr12:106617649 | A | G | 1 | a0001c0002t0001g0252 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.130+8766A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617649 | |||||||
| chr12:106617675 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+8792C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617675 | |||||||
| chr12:106617793 | C | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+8910C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617793 | |||||||
| chr12:106617938 | G | T | 1 | a0001c0001t0001g0024 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.130+9055G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617938 | |||||||
| chr12:106617950 | C | T | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130+9067C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106617950 | |||||||
| chr12:106618177 | C | A | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.130+9294C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106618177 | |||||||
| chr12:106618179 | T | TTATAGAT others(14): Show |
3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.130+9314_130+9334d others(23): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106618179 | ||||||
| chr12:106618221 | TATATGTT others(9): Show |
T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+9352_130+9367d others(18): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106618221 | ||||||
| chr12:106618247 | A | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.130+9364A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106618247 | |||||||
| chr12:106618429 | A | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.130+9546A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106618429 | |||||||
| chr12:106618595 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.130+9712T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106618595 | |||||||
| chr12:106618647 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.130+9764C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106618647 | |||||||
| chr12:106618958 | A | C | 1 | a0001c0002t0001g0015 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.130+10075A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106618958 | |||||||
| chr12:106619007 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.130+10124T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106619007 | |||||||
| chr12:106619093 | A | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.130+10210A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106619093 | |||||||
| chr12:106619191 | C | T | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130+10308C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106619191 | |||||||
| chr12:106619685 | A | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(99): Show |
103 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.130+10802A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106619685 | |||||||
| chr12:106619710 | A | T | 27 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(24): Show |
27 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.130+10827A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106619710 | |||||||
| chr12:106619743 | T | A | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.130+10860T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106619743 | |||||||
| chr12:106619761 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.130+10878G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106619761 | |||||||
| chr12:106619834 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.130+10951C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106619834 | |||||||
| chr12:106620234 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.130+11351G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106620234 | |||||||
| chr12:106620260 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.130+11377G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106620260 | |||||||
| chr12:106620394 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.130+11511A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106620394 | |||||||
| chr12:106620539 | ACAAAGGG others(43): Show |
A | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.130+11683_130+1173 others(54): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106620539 | ||||||
| chr12:106620636 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.130+11753G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106620636 | |||||||
| chr12:106620945 | C | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.130+12062C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106620945 | |||||||
| chr12:106621030 | G | A | 3 | a0001c0002t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0228 |
3 | HG01167.hp1 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.130+12147G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621030 | |||||||
| chr12:106621155 | G | A | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130+12272G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621155 | |||||||
| chr12:106621259 | C | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+12376C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621259 | |||||||
| chr12:106621477 | C | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.130+12594C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621477 | |||||||
| chr12:106621491 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(30): Show |
34 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.130+12608C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621491 | |||||||
| chr12:106621607 | A | G | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130+12724A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621607 | |||||||
| chr12:106621724 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.130+12841A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621724 | |||||||
| chr12:106621726 | C | A | 1 | a0001c0002t0001g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.130+12843C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621726 | |||||||
| chr12:106621773 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.130+12890C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621773 | |||||||
| chr12:106621793 | TGGAAAGA others(7): Show |
T | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130+12923_130+1293 others(18): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106621793 | ||||||
| chr12:106621807 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.130+12924G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621807 | |||||||
| chr12:106621821 | G | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+12938G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621821 | |||||||
| chr12:106621869 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.130+12986C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106621869 | |||||||
| chr12:106622155 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(30): Show |
34 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.130+13272G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622155 | |||||||
| chr12:106622226 | T | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0035 others(42): Show |
45 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.130+13343T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622226 | |||||||
| chr12:106622330 | G | A | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+13447G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622330 | |||||||
| chr12:106622430 | A | T | 1 | a0001c0001t0001g0281 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.130+13547A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622430 | |||||||
| chr12:106622622 | A | AT | 15 | a0001c0001t0001g0088 a0001c0001t0001g0161 a0001c0001t0001g0202 others(12): Show |
15 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+13757dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106622622 | ||||||
| chr12:106622622 | AT | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.130+13757delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106622622 | ||||||
| chr12:106622622 | ATT | A | 7 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(4): Show |
7 | HG01243.hp1 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+13756_130+1375 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106622622 | ||||||
| chr12:106622624 | T | C | 6 | a0001c0002t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0109 others(3): Show |
6 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+13741T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622624 | |||||||
| chr12:106622625 | T | C | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130+13742T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622625 | |||||||
| chr12:106622628 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.130+13745T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622628 | |||||||
| chr12:106622654 | G | T | 1 | a0001c0002t0001g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.130+13771G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622654 | |||||||
| chr12:106622669 | A | G | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.130+13786A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622669 | |||||||
| chr12:106622730 | C | T | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.130+13847C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622730 | |||||||
| chr12:106622910 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.130+14027G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622910 | |||||||
| chr12:106622939 | CT | C | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.130+14057delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622939 | |||||||
| chr12:106622964 | A | G | 1 | a0001c0002t0001g0184 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+14081A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106622964 | |||||||
| chr12:106623037 | C | CT | 10 | a0001c0001t0001g0111 a0001c0001t0001g0161 a0001c0001t0001g0217 others(7): Show |
10 | HG01081.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+14173dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106623037 | ||||||
| chr12:106623037 | CT | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0106 a0001c0001t0001g0118 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.130+14173delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106623037 | ||||||
| chr12:106623037 | CTT | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0035 others(34): Show |
37 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.130+14172_130+1417 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106623037 | ||||||
| chr12:106623229 | A | G | 6 | a0001c0001t0001g0087 a0001c0001t0001g0103 a0001c0001t0001g0105 others(3): Show |
6 | HG01952.hp2 HG02486.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+14346A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623229 | |||||||
| chr12:106623239 | G | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0196 a0001c0001t0001g0206 others(3): Show |
6 | HG00735.hp1 HG01069.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+14356G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623239 | |||||||
| chr12:106623387 | G | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0234 |
2 | NA18942.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.130+14504G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623387 | |||||||
| chr12:106623416 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.130+14533T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623416 | |||||||
| chr12:106623425 | A | G | 1 | a0001c0002t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.130+14542A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623425 | |||||||
| chr12:106623689 | T | C | 3 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0003c0006t0001g0116 |
3 | HG02630.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.130+14806T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623689 | |||||||
| chr12:106623718 | G | A | 1 | a0001c0003t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.130+14835G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623718 | |||||||
| chr12:106623777 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0293 |
2 | HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.130+14894C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623777 | |||||||
| chr12:106623833 | C | T | 3 | a0001c0001t0001g0003 a0001c0002t0005g0061 a0002c0005t0001g0062 |
3 | HG01943.hp2 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130+14950C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623833 | |||||||
| chr12:106623892 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.130+15009T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623892 | |||||||
| chr12:106623954 | T | G | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.130+15071T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623954 | |||||||
| chr12:106623985 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.130+15102C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623985 | |||||||
| chr12:106623995 | T | C | 4 | a0001c0001t0001g0131 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+15112T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106623995 | |||||||
| chr12:106624241 | A | C | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.131-15091A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106624241 | |||||||
| chr12:106624318 | A | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(25): Show |
28 | HG00609.hp1 HG01109.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-15014A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106624318 | |||||||
| chr12:106624369 | G | A | 1 | a0001c0002t0001g0237 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.131-14963G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106624369 | |||||||
| chr12:106624475 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.131-14857C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106624475 | |||||||
| chr12:106624922 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.131-14410C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106624922 | |||||||
| chr12:106624994 | T | C | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.131-14338T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106624994 | |||||||
| chr12:106625190 | A | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0088 others(62): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.131-14142A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106625190 | |||||||
| chr12:106625385 | C | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.131-13947C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106625385 | |||||||
| chr12:106625406 | G | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.131-13926G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106625406 | |||||||
| chr12:106625458 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.131-13874C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106625458 | |||||||
| chr12:106626066 | A | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.131-13266A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106626066 | |||||||
| chr12:106626073 | A | T | 27 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(24): Show |
27 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.131-13259A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106626073 | |||||||
| chr12:106626112 | T | C | 1 | a0001c0003t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.131-13220T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106626112 | |||||||
| chr12:106626306 | A | G | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-13026A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106626306 | |||||||
| chr12:106626437 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.131-12895A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106626437 | |||||||
| chr12:106626619 | G | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0035 others(56): Show |
59 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.131-12713G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106626619 | |||||||
| chr12:106626895 | C | T | 2 | a0001c0001t0001g0149 a0001c0002t0001g0068 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.131-12437C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106626895 | |||||||
| chr12:106626925 | C | T | 14 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(11): Show |
14 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-12407C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106626925 | |||||||
| chr12:106627023 | C | T | 47 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(44): Show |
47 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.131-12309C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106627023 | |||||||
| chr12:106627138 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.131-12194C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106627138 | |||||||
| chr12:106627151 | T | C | 3 | a0001c0001t0001g0003 a0001c0002t0005g0061 a0002c0005t0001g0062 |
3 | HG01943.hp2 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.131-12181T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106627151 | |||||||
| chr12:106627155 | A | G | 14 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(11): Show |
14 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-12177A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106627155 | |||||||
| chr12:106627353 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 |
3 | HG01258.hp2 HG01517.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.131-11979G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106627353 | |||||||
| chr12:106627449 | T | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.131-11883T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106627449 | |||||||
| chr12:106627671 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.131-11661C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106627671 | |||||||
| chr12:106627750 | C | T | 3 | a0001c0002t0001g0165 a0001c0002t0001g0180 a0001c0002t0001g0185 |
3 | HG01256.hp2 HG03704.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.131-11582C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106627750 | |||||||
| chr12:106627943 | A | T | 14 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(11): Show |
14 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-11389A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106627943 | |||||||
| chr12:106628060 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0002t0001g0002 others(54): Show |
57 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.131-11272A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628060 | |||||||
| chr12:106628160 | C | T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0077 others(29): Show |
32 | HG00408.hp1 HG00438.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.131-11172C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628160 | |||||||
| chr12:106628191 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.131-11141C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628191 | |||||||
| chr12:106628358 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.131-10974T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628358 | |||||||
| chr12:106628580 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-10752G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628580 | |||||||
| chr12:106628655 | A | G | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.131-10677A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628655 | |||||||
| chr12:106628673 | C | G | 2 | a0001c0002t0001g0120 a0001c0002t0001g0122 |
2 | HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.131-10659C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628673 | |||||||
| chr12:106628762 | C | CTT | 33 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(30): Show |
34 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.131-10554_131-1055 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106628762 | ||||||
| chr12:106628762 | CT | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0001t0001g0260 others(46): Show |
49 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.131-10553delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106628762 | ||||||
| chr12:106628849 | T | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.131-10483T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628849 | |||||||
| chr12:106628860 | A | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0002t0001g0017 others(49): Show |
52 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.131-10472A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628860 | |||||||
| chr12:106628996 | T | A | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.131-10336T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106628996 | |||||||
| chr12:106629283 | C | T | 1 | a0001c0002t0001g0015 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-10049C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106629283 | |||||||
| chr12:106629325 | T | C | 1 | a0001c0002t0001g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.131-10007T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106629325 | |||||||
| chr12:106629827 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.131-9505C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106629827 | |||||||
| chr12:106629834 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0208 |
2 | HG00609.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.131-9498A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106629834 | |||||||
| chr12:106629902 | C | G | 6 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 others(3): Show |
6 | HG00609.hp1 HG01099.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-9430C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106629902 | |||||||
| chr12:106629924 | G | A | 6 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG01123.hp2 HG01433.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-9408G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106629924 | |||||||
| chr12:106630031 | A | G | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.131-9301A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106630031 | |||||||
| chr12:106630560 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.131-8772C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106630560 | |||||||
| chr12:106630561 | G | A | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0181 others(2): Show |
5 | HG02155.hp1 NA18948.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-8771G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106630561 | |||||||
| chr12:106630585 | G | A | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.131-8747G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106630585 | |||||||
| chr12:106630783 | C | T | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.131-8549C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106630783 | |||||||
| chr12:106631045 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.131-8287C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631045 | |||||||
| chr12:106631159 | C | G | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.131-8173C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631159 | |||||||
| chr12:106631160 | A | T | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.131-8172A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631160 | |||||||
| chr12:106631365 | G | T | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.131-7967G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631365 | |||||||
| chr12:106631416 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.131-7916G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631416 | |||||||
| chr12:106631694 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.131-7638C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631694 | |||||||
| chr12:106631732 | A | G | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-7600A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631732 | |||||||
| chr12:106631816 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.131-7516C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631816 | |||||||
| chr12:106631920 | A | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.131-7412A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631920 | |||||||
| chr12:106631964 | T | A | 1 | a0001c0002t0001g0063 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.131-7368T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106631964 | |||||||
| chr12:106632076 | C | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0282 |
2 | HG01074.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.131-7256C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106632076 | |||||||
| chr12:106632285 | GT | G | 8 | a0001c0001t0001g0262 a0001c0002t0001g0058 a0001c0002t0001g0059 others(5): Show |
8 | HG01167.hp1 HG01433.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-7037delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106632285 | ||||||
| chr12:106632337 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.131-6995G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106632337 | |||||||
| chr12:106632581 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.131-6751T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106632581 | |||||||
| chr12:106632596 | G | C | 6 | a0001c0001t0001g0149 a0001c0002t0001g0068 a0001c0003t0001g0141 others(3): Show |
6 | HG01109.hp2 HG02486.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-6736G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106632596 | |||||||
| chr12:106632597 | C | G | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.131-6735C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106632597 | |||||||
| chr12:106632706 | A | G | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.131-6626A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106632706 | |||||||
| chr12:106632837 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.131-6495G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106632837 | |||||||
| chr12:106632883 | G | A | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.131-6449G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106632883 | |||||||
| chr12:106632937 | C | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-6395C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106632937 | |||||||
| chr12:106633009 | C | T | 4 | a0001c0003t0001g0009 a0001c0003t0001g0072 a0001c0003t0001g0073 others(1): Show |
4 | HG01175.hp1 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-6323C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633009 | |||||||
| chr12:106633039 | T | A | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-6293T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633039 | |||||||
| chr12:106633040 | A | C | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-6292A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633040 | |||||||
| chr12:106633042 | A | C | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-6290A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633042 | |||||||
| chr12:106633046 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-6286C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633046 | |||||||
| chr12:106633047 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-6285C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633047 | |||||||
| chr12:106633048 | A | C | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-6284A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633048 | |||||||
| chr12:106633061 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-6271A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633061 | |||||||
| chr12:106633062 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-6270A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633062 | |||||||
| chr12:106633063 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-6269C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633063 | |||||||
| chr12:106633188 | C | T | 4 | a0001c0001t0001g0159 a0001c0001t0001g0207 a0001c0001t0001g0246 others(1): Show |
4 | NA18982.hp2 NA19054.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-6144C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633188 | |||||||
| chr12:106633332 | A | G | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.131-6000A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633332 | |||||||
| chr12:106633338 | T | G | 2 | a0001c0003t0001g0109 a0001c0003t0001g0110 |
2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.131-5994T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633338 | |||||||
| chr12:106633513 | A | C | 7 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0003t0001g0060 others(4): Show |
7 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-5819A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633513 | |||||||
| chr12:106633555 | A | T | 1 | a0001c0001t0001g0283 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.131-5777A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633555 | |||||||
| chr12:106633634 | A | G | 3 | a0001c0002t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0228 |
3 | HG01167.hp1 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.131-5698A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633634 | |||||||
| chr12:106633652 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.131-5680G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633652 | |||||||
| chr12:106633660 | T | G | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-5672T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633660 | |||||||
| chr12:106633661 | G | T | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.131-5671G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633661 | |||||||
| chr12:106633737 | C | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0266 |
2 | NA18990.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.131-5595C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633737 | |||||||
| chr12:106633870 | C | A | 40 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0177 others(37): Show |
40 | HG00438.hp1 HG00621.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.131-5462C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106633870 | |||||||
| chr12:106634033 | T | C | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.131-5299T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106634033 | |||||||
| chr12:106634130 | C | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0118 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.131-5202C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106634130 | |||||||
| chr12:106634191 | A | G | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.131-5141A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106634191 | |||||||
| chr12:106634554 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.131-4778G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106634554 | |||||||
| chr12:106634608 | T | C | 7 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0003t0001g0060 others(4): Show |
7 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-4724T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106634608 | |||||||
| chr12:106634742 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.131-4590C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106634742 | |||||||
| chr12:106635007 | A | G | 44 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(41): Show |
44 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.131-4325A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635007 | |||||||
| chr12:106635035 | A | G | 1 | a0001c0002t0001g0133 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.131-4297A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635035 | |||||||
| chr12:106635211 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(71): Show |
75 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.131-4121C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635211 | |||||||
| chr12:106635286 | T | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(24): Show |
28 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.131-4046T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635286 | |||||||
| chr12:106635302 | A | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.131-4030A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635302 | |||||||
| chr12:106635344 | T | C | 1 | a0001c0002t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131-3988T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635344 | |||||||
| chr12:106635419 | T | C | 1 | a0001c0002t0001g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.131-3913T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635419 | |||||||
| chr12:106635429 | T | A | 37 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(34): Show |
37 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.131-3903T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635429 | |||||||
| chr12:106635499 | G | C | 1 | a0001c0001t0001g0005 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.131-3833G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635499 | |||||||
| chr12:106635686 | T | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(18): Show |
22 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-3646T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635686 | |||||||
| chr12:106635925 | A | G | 7 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0003t0001g0060 others(4): Show |
7 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-3407A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106635925 | |||||||
| chr12:106636390 | C | CAA | 35 | a0001c0001t0001g0149 a0001c0002t0001g0017 a0001c0002t0001g0018 others(32): Show |
35 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.131-2926_131-2925d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106636390 | ||||||
| chr12:106636390 | CA | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0002t0006g0147 others(8): Show |
11 | HG01175.hp1 HG01943.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-2925delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106636390 | ||||||
| chr12:106636475 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.131-2857A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106636475 | |||||||
| chr12:106636506 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.131-2826T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106636506 | |||||||
| chr12:106636775 | A | G | 41 | a0001c0001t0001g0100 a0001c0002t0001g0013 a0001c0002t0001g0014 others(38): Show |
41 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.131-2557A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106636775 | |||||||
| chr12:106636865 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.131-2467T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106636865 | |||||||
| chr12:106637038 | G | C | 1 | a0001c0002t0001g0225 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.131-2294G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106637038 | |||||||
| chr12:106637525 | A | G | 6 | a0001c0001t0001g0149 a0001c0002t0001g0068 a0001c0003t0001g0141 others(3): Show |
6 | HG01109.hp2 HG02486.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-1807A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106637525 | |||||||
| chr12:106637673 | AG | A | 44 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(41): Show |
44 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.131-1657delG | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106637673 | ||||||
| chr12:106637697 | T | C | 1 | a0001c0002t0001g0235 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.131-1635T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106637697 | |||||||
| chr12:106638017 | AT | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0150 a0001c0001t0001g0151 others(11): Show |
14 | HG01175.hp1 HG01943.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-1301delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106638017 | ||||||
| chr12:106638040 | C | T | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.131-1292C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106638040 | |||||||
| chr12:106638251 | A | T | 2 | a0001c0002t0001g0176 a0001c0002t0001g0240 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.131-1081A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106638251 | |||||||
| chr12:106638267 | G | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0002t0001g0002 others(62): Show |
65 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.131-1065G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106638267 | |||||||
| chr12:106638396 | A | G | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.131-936A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106638396 | |||||||
| chr12:106638491 | A | AACACTT | 65 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0002t0001g0002 others(62): Show |
65 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.131-840_131-835dup others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr12 | 106638491 | ||||||
| chr12:106638898 | T | G | 1 | a0001c0002t0001g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.131-434T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106638898 | |||||||
| chr12:106638912 | G | T | 2 | a0001c0001t0001g0003 a0002c0005t0001g0062 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.131-420G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106638912 | |||||||
| chr12:106638922 | G | T | 1 | a0001c0001t0001g0271 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.131-410G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106638922 | |||||||
| chr12:106638930 | A | G | 7 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0003t0001g0060 others(4): Show |
7 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-402A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106638930 | |||||||
| chr12:106639096 | A | G | 6 | a0001c0002t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0109 others(3): Show |
6 | HG01167.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-236A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106639096 | |||||||
| chr12:106639269 | A | G | 40 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(37): Show |
40 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.131-63A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 2/17 | chr12 | 106639269 | |||||||
| chr12:106639468 | T | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.191+76T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106639468 | |||||||
| chr12:106639536 | T | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0002t0001g0068 others(12): Show |
15 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.191+144T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106639536 | |||||||
| chr12:106639775 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0002t0001g0068 others(12): Show |
15 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.191+383A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106639775 | |||||||
| chr12:106639886 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.191+494A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106639886 | |||||||
| chr12:106639896 | A | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.191+504A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106639896 | |||||||
| chr12:106640249 | A | T | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+857A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106640249 | |||||||
| chr12:106640305 | C | A | 1 | a0001c0002t0001g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.191+913C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106640305 | |||||||
| chr12:106640383 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0002t0001g0068 others(13): Show |
16 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.191+991G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106640383 | |||||||
| chr12:106640618 | T | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.191+1226T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106640618 | |||||||
| chr12:106640639 | T | C | 1 | a0001c0002t0001g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.191+1247T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106640639 | |||||||
| chr12:106640778 | C | CT | 21 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0149 others(18): Show |
21 | HG00741.hp1 HG01169.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.191+1406dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106640778 | ||||||
| chr12:106640778 | C | CTT | 36 | a0001c0002t0001g0021 a0001c0002t0001g0032 a0001c0002t0001g0033 others(33): Show |
36 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.191+1405_191+1406d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106640778 | ||||||
| chr12:106640778 | CT | C | 16 | a0001c0001t0001g0087 a0001c0001t0001g0095 a0001c0001t0001g0103 others(13): Show |
16 | HG01099.hp2 HG01167.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.191+1406delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106640778 | ||||||
| chr12:106640793 | T | TC | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.191+1401_191+1402i others(3): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106640793 | |||||||
| chr12:106640819 | C | T | 3 | a0001c0002t0001g0165 a0001c0002t0001g0180 a0001c0002t0001g0185 |
3 | HG01256.hp2 HG03704.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.191+1427C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106640819 | |||||||
| chr12:106640820 | G | A | 3 | a0001c0002t0001g0157 a0001c0002t0001g0179 a0001c0002t0001g0192 |
3 | HG01884.hp1 HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.191+1428G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106640820 | |||||||
| chr12:106640842 | G | T | 15 | a0001c0001t0001g0149 a0001c0002t0001g0068 a0001c0003t0001g0009 others(12): Show |
15 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.191+1450G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106640842 | |||||||
| chr12:106641072 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.191+1680T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641072 | |||||||
| chr12:106641113 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.191+1721G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641113 | |||||||
| chr12:106641590 | C | T | 2 | a0001c0002t0001g0056 a0001c0002t0001g0057 |
2 | HG01168.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.191+2198C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641590 | |||||||
| chr12:106641815 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.191+2423A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641815 | |||||||
| chr12:106641816 | T | C | 24 | a0001c0002t0001g0021 a0001c0002t0001g0032 a0001c0002t0001g0033 others(21): Show |
24 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.191+2424T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641816 | |||||||
| chr12:106641935 | A | G | 41 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(38): Show |
41 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.191+2543A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641935 | |||||||
| chr12:106641951 | C | CTATCTA | 4 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+2573_191+2578d others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641951 | ||||||
| chr12:106641951 | C | CTATCTAT others(5): Show |
3 | a0001c0001t0001g0149 a0001c0002t0001g0068 a0001c0003t0001g0072 |
3 | HG02486.hp1 HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.191+2567_191+2578d others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641951 | ||||||
| chr12:106641951 | C | CTATCTAT others(11): Show |
3 | a0001c0004t0001g0012 a0001c0004t0001g0101 a0003c0006t0001g0116 |
3 | HG02486.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.191+2561_191+2578d others(20): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641951 | ||||||
| chr12:106641951 | CTATCTA | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+2573_191+2578d others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641951 | ||||||
| chr12:106641957 | ATATCTAT others(3): Show |
A | 1 | a0001c0002t0001g0037 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.191+2579_191+2588d others(12): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641957 | ||||||
| chr12:106641961 | CTATATCT others(5): Show |
C | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.191+2573_191+2584d others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641961 | ||||||
| chr12:106641963 | ATATC | A | 34 | a0001c0002t0001g0021 a0001c0002t0001g0029 a0001c0002t0001g0032 others(31): Show |
34 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.191+2579_191+2582d others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641963 | ||||||
| chr12:106641965 | A | C | 2 | a0001c0001t0001g0024 a0001c0002t0005g0061 |
2 | HG01361.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.191+2573A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641965 | |||||||
| chr12:106641967 | C | A | 4 | a0001c0001t0001g0024 a0001c0002t0001g0070 a0001c0002t0001g0071 others(1): Show |
4 | HG01361.hp1 HG02109.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+2575C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641967 | |||||||
| chr12:106641967 | C | CTATATCT others(1): Show |
5 | a0001c0002t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0110 others(2): Show |
5 | HG01167.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.191+2578_191+2579i others(10): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | C | CTATATCT others(11): Show |
2 | a0001c0003t0001g0073 a0001c0003t0001g0074 |
2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.191+2578_191+2579i others(20): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | C | CTATATCT others(23): Show |
1 | a0001c0003t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.191+2578_191+2579i others(32): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | C | CTATATCT others(5): Show |
1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.191+2578_191+2579i others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | C | CTATCTA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.191+2625_191+2630d others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | C | CTATCTAT others(5): Show |
30 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0022 others(27): Show |
30 | HG00140.hp1 HG01071.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.191+2619_191+2630d others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | C | CTATCTAT others(11): Show |
6 | a0001c0001t0001g0025 a0001c0001t0001g0055 a0001c0001t0001g0089 others(3): Show |
6 | HG02622.hp1 HG02809.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+2613_191+2630d others(20): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | C | CTATCTAT others(17): Show |
2 | a0001c0001t0001g0026 a0001c0002t0001g0135 |
2 | HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.191+2607_191+2630d others(26): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | CTATCTA | C | 23 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0103 others(20): Show |
23 | HG00438.hp1 HG00621.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.191+2625_191+2630d others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | CTATCTAT others(5): Show |
C | 7 | a0001c0001t0001g0087 a0001c0001t0001g0149 a0001c0001t0001g0159 others(4): Show |
7 | HG02486.hp1 HG03041.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.191+2619_191+2630d others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | CTATCTAT others(11): Show |
C | 4 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0068 others(1): Show |
4 | HG00609.hp1 HG02027.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+2613_191+2630d others(20): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641967 | CTATCTAT others(17): Show |
C | 1 | a0001c0002t0001g0258 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.191+2607_191+2630d others(26): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641967 | ||||||
| chr12:106641971 | C | A | 6 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(3): Show |
6 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+2579C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641971 | |||||||
| chr12:106641973 | A | ATATC | 5 | a0001c0002t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0110 others(2): Show |
5 | HG01167.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.191+2585_191+2588d others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641973 | ||||||
| chr12:106641973 | A | C | 6 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(3): Show |
6 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+2581A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106641973 | |||||||
| chr12:106641977 | CTA | C | 30 | a0001c0002t0001g0021 a0001c0002t0001g0029 a0001c0002t0001g0032 others(27): Show |
30 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.191+2589_191+2590d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641977 | ||||||
| chr12:106641983 | CTA | C | 5 | a0001c0002t0001g0037 a0001c0003t0001g0141 a0001c0003t0001g0143 others(2): Show |
5 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.191+2595_191+2596d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106641983 | ||||||
| chr12:106642156 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.191+2764A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106642156 | |||||||
| chr12:106642278 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.191+2886A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106642278 | |||||||
| chr12:106642292 | G | A | 40 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(37): Show |
40 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.191+2900G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106642292 | |||||||
| chr12:106642306 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.191+2914G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106642306 | |||||||
| chr12:106642329 | T | G | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.191+2937T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106642329 | |||||||
| chr12:106642351 | C | T | 15 | a0001c0002t0001g0059 a0001c0003t0001g0009 a0001c0003t0001g0060 others(12): Show |
15 | HG01167.hp1 HG01175.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.191+2959C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106642351 | |||||||
| chr12:106642531 | G | A | 29 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(26): Show |
29 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.191+3139G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106642531 | |||||||
| chr12:106642775 | G | A | 10 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.191+3383G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106642775 | |||||||
| chr12:106642799 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.191+3407G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106642799 | |||||||
| chr12:106643047 | G | A | 2 | a0001c0001t0001g0149 a0001c0002t0001g0068 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.191+3655G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106643047 | |||||||
| chr12:106643075 | A | G | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.191+3683A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106643075 | |||||||
| chr12:106643106 | T | C | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.191+3714T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106643106 | |||||||
| chr12:106643161 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.191+3769C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106643161 | |||||||
| chr12:106643201 | G | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.191+3809G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106643201 | |||||||
| chr12:106643265 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.191+3873G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106643265 | |||||||
| chr12:106643323 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.191+3931G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106643323 | |||||||
| chr12:106643547 | T | A | 30 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(27): Show |
30 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.191+4155T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106643547 | |||||||
| chr12:106643627 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.191+4235T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106643627 | |||||||
| chr12:106644078 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0245 |
2 | HG00741.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.191+4686G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106644078 | |||||||
| chr12:106644230 | C | CT | 13 | a0001c0001t0001g0016 a0001c0001t0001g0152 a0001c0001t0001g0167 others(10): Show |
13 | HG00140.hp2 HG00738.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.191+4859dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106644230 | ||||||
| chr12:106644230 | CT | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(24): Show |
28 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.191+4859delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106644230 | ||||||
| chr12:106644260 | G | A | 5 | a0001c0003t0001g0060 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.191+4868G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106644260 | |||||||
| chr12:106644393 | C | T | 3 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0003c0006t0001g0116 |
3 | HG02630.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.191+5001C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106644393 | |||||||
| chr12:106644484 | C | T | 1 | a0001c0001t0004g0036 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.191+5092C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106644484 | |||||||
| chr12:106644496 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.191+5104G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106644496 | |||||||
| chr12:106644603 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02257.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.191+5211G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106644603 | |||||||
| chr12:106644857 | A | G | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.191+5465A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106644857 | |||||||
| chr12:106644910 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.191+5518C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106644910 | |||||||
| chr12:106644958 | T | C | 20 | a0001c0001t0001g0149 a0001c0002t0001g0068 a0001c0003t0001g0009 others(17): Show |
20 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.191+5566T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106644958 | |||||||
| chr12:106645024 | G | C | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.191+5632G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645024 | |||||||
| chr12:106645041 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.191+5649C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645041 | |||||||
| chr12:106645041 | C | T | 3 | a0001c0002t0001g0002 a0001c0002t0001g0049 a0001c0002t0001g0083 |
3 | HG00609.hp1 HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.191+5649C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645041 | |||||||
| chr12:106645052 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG02615.hp1 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.191+5660A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645052 | |||||||
| chr12:106645094 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.191+5702G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645094 | |||||||
| chr12:106645276 | A | T | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.191+5884A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645276 | |||||||
| chr12:106645346 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.191+5954C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645346 | |||||||
| chr12:106645497 | G | A | 1 | a0001c0003t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.191+6105G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645497 | |||||||
| chr12:106645607 | T | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.191+6215T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645607 | |||||||
| chr12:106645686 | C | T | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.191+6294C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645686 | |||||||
| chr12:106645815 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0103 a0001c0001t0001g0105 |
3 | HG03041.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.191+6423G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106645815 | |||||||
| chr12:106646007 | C | T | 5 | a0001c0001t0001g0131 a0001c0002t0001g0124 a0001c0002t0001g0125 others(2): Show |
5 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.191+6615C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646007 | |||||||
| chr12:106646021 | A | T | 3 | a0001c0001t0001g0233 a0001c0002t0001g0070 a0001c0002t0001g0071 |
3 | HG02723.hp2 HG02976.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.191+6629A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646021 | |||||||
| chr12:106646059 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.191+6667G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646059 | |||||||
| chr12:106646181 | T | C | 41 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(38): Show |
41 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.191+6789T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646181 | |||||||
| chr12:106646183 | C | T | 36 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0031 others(33): Show |
36 | HG00438.hp1 HG00621.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.191+6791C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646183 | |||||||
| chr12:106646244 | T | G | 29 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(26): Show |
29 | HG00408.hp2 HG00639.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.191+6852T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646244 | |||||||
| chr12:106646263 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.191+6871A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646263 | |||||||
| chr12:106646335 | C | T | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.191+6943C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646335 | |||||||
| chr12:106646378 | C | T | 20 | a0001c0001t0001g0149 a0001c0002t0001g0068 a0001c0003t0001g0009 others(17): Show |
20 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.191+6986C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646378 | |||||||
| chr12:106646382 | A | G | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+6990A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646382 | |||||||
| chr12:106646431 | C | CA | 17 | a0001c0001t0001g0113 a0001c0001t0001g0198 a0001c0001t0001g0230 others(14): Show |
17 | HG00735.hp1 HG01081.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.191+7067dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106646431 | ||||||
| chr12:106646431 | C | CAA | 22 | a0001c0002t0001g0017 a0001c0002t0001g0021 a0001c0002t0001g0029 others(19): Show |
22 | HG00639.hp1 HG01074.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.191+7066_191+7067d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106646431 | ||||||
| chr12:106646431 | CA | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.191+7067delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106646431 | ||||||
| chr12:106646431 | CAA | C | 10 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0087 others(7): Show |
10 | HG00738.hp2 HG00741.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.191+7066_191+7067d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106646431 | ||||||
| chr12:106646431 | CAAAAA | C | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG01109.hp2 HG01361.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.191+7063_191+7067d others(7): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106646431 | ||||||
| chr12:106646431 | CAAAAAAA others(2): Show |
C | 8 | a0001c0002t0001g0034 a0001c0002t0001g0038 a0001c0002t0001g0039 others(5): Show |
8 | HG00408.hp2 HG02056.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.191+7059_191+7067d others(11): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106646431 | ||||||
| chr12:106646431 | CAAAAAAA others(4): Show |
C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.191+7057_191+7067d others(13): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106646431 | ||||||
| chr12:106646458 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.191+7066A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646458 | |||||||
| chr12:106646564 | G | A | 18 | a0001c0003t0001g0009 a0001c0003t0001g0060 a0001c0003t0001g0072 others(15): Show |
18 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.191+7172G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646564 | |||||||
| chr12:106646664 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.191+7272G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646664 | |||||||
| chr12:106646875 | C | T | 3 | a0001c0001t0001g0149 a0001c0002t0001g0068 a0001c0002t0006g0147 |
3 | HG02486.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.192-7353C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646875 | |||||||
| chr12:106646923 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.192-7305C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646923 | |||||||
| chr12:106646946 | G | A | 3 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0003t0001g0019 |
3 | HG02922.hp1 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.192-7282G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106646946 | |||||||
| chr12:106647173 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.192-7055T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106647173 | |||||||
| chr12:106647209 | A | G | 2 | a0001c0002t0001g0135 a0001c0002t0005g0061 |
2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192-7019A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106647209 | |||||||
| chr12:106647309 | T | TC | 4 | a0001c0003t0001g0009 a0001c0003t0001g0072 a0001c0003t0001g0073 others(1): Show |
4 | HG01175.hp1 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-6916dupC | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106647309 | ||||||
| chr12:106647322 | G | A | 5 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0072 others(2): Show |
5 | HG01175.hp1 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-6906G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106647322 | |||||||
| chr12:106647382 | T | C | 3 | a0001c0002t0001g0042 a0001c0002t0001g0044 a0001c0002t0001g0046 |
3 | HG01081.hp1 HG01106.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.192-6846T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106647382 | |||||||
| chr12:106647400 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.192-6828T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106647400 | |||||||
| chr12:106647434 | C | T | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-6794C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106647434 | |||||||
| chr12:106647678 | A | C | 83 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0001c0002t0001g0002 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.192-6550A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106647678 | |||||||
| chr12:106648004 | A | T | 39 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0031 others(36): Show |
39 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.192-6224A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106648004 | |||||||
| chr12:106648304 | A | C | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192-5924A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106648304 | |||||||
| chr12:106648488 | G | GT | 10 | a0001c0001t0001g0112 a0001c0001t0001g0150 a0001c0001t0001g0151 others(7): Show |
10 | HG01934.hp2 HG02572.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.192-5728dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106648488 | ||||||
| chr12:106648489 | T | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG01516.hp1 HG01517.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.192-5739T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106648489 | |||||||
| chr12:106648604 | T | TA | 10 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(7): Show |
10 | HG01168.hp1 HG01169.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.192-5612dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106648604 | ||||||
| chr12:106648604 | T | TAA | 11 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0060 others(8): Show |
11 | HG01175.hp1 HG01943.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.192-5613_192-5612d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106648604 | ||||||
| chr12:106648622 | T | TG | 4 | a0001c0001t0001g0243 a0001c0003t0001g0019 a0001c0003t0001g0143 others(1): Show |
4 | HG01109.hp2 HG01943.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-5602dupG | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106648622 | ||||||
| chr12:106648626 | G | GT | 37 | a0001c0001t0001g0086 a0001c0001t0001g0105 a0001c0001t0001g0112 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.192-5584dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106648626 | ||||||
| chr12:106648626 | G | T | 2 | a0001c0002t0001g0127 a0001c0002t0001g0130 |
2 | HG02145.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.192-5602G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106648626 | |||||||
| chr12:106648626 | GT | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0107 others(3): Show |
6 | HG01258.hp2 HG01884.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-5584delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106648626 | ||||||
| chr12:106648627 | T | G | 8 | a0001c0002t0001g0017 a0001c0003t0001g0009 a0001c0003t0001g0072 others(5): Show |
8 | HG01175.hp1 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.192-5601T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106648627 | |||||||
| chr12:106648685 | G | T | 96 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(93): Show |
96 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.192-5543G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106648685 | |||||||
| chr12:106648725 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0170 others(3): Show |
6 | HG01243.hp2 HG02056.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-5503C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106648725 | |||||||
| chr12:106648800 | A | G | 86 | a0001c0001t0001g0149 a0001c0002t0001g0002 a0001c0002t0001g0013 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.192-5428A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106648800 | |||||||
| chr12:106648978 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.192-5250C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106648978 | |||||||
| chr12:106649113 | C | T | 15 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0060 others(12): Show |
15 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.192-5115C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106649113 | |||||||
| chr12:106649289 | C | G | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.192-4939C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106649289 | |||||||
| chr12:106649525 | C | T | 86 | a0001c0001t0001g0149 a0001c0002t0001g0002 a0001c0002t0001g0013 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.192-4703C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106649525 | |||||||
| chr12:106649594 | A | G | 20 | a0001c0002t0006g0147 a0001c0003t0001g0009 a0001c0003t0001g0019 others(17): Show |
20 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.192-4634A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106649594 | |||||||
| chr12:106649654 | A | G | 86 | a0001c0001t0001g0149 a0001c0002t0001g0002 a0001c0002t0001g0013 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.192-4574A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106649654 | |||||||
| chr12:106649879 | T | C | 7 | a0001c0001t0001g0113 a0001c0001t0001g0196 a0001c0001t0001g0206 others(4): Show |
7 | HG00735.hp1 HG01069.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.192-4349T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106649879 | |||||||
| chr12:106650079 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192-4149C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106650079 | |||||||
| chr12:106650111 | T | G | 7 | a0001c0002t0001g0034 a0001c0002t0001g0039 a0001c0002t0001g0040 others(4): Show |
7 | HG00408.hp2 NA18939.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-4117T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106650111 | |||||||
| chr12:106650251 | T | A | 1 | a0001c0002t0001g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.192-3977T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106650251 | |||||||
| chr12:106650314 | C | T | 63 | a0001c0001t0001g0149 a0001c0002t0001g0013 a0001c0002t0001g0014 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.192-3914C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106650314 | |||||||
| chr12:106650389 | C | A | 49 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.192-3839C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106650389 | |||||||
| chr12:106650503 | T | C | 86 | a0001c0001t0001g0149 a0001c0002t0001g0002 a0001c0002t0001g0013 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.192-3725T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106650503 | |||||||
| chr12:106650660 | G | A | 6 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0001g0187 others(3): Show |
6 | HG00438.hp1 HG00621.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-3568G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106650660 | |||||||
| chr12:106650678 | A | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.192-3550A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106650678 | |||||||
| chr12:106650893 | T | C | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.192-3335T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106650893 | |||||||
| chr12:106651006 | A | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.192-3222A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106651006 | |||||||
| chr12:106651106 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192-3122A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106651106 | |||||||
| chr12:106651451 | CTGT | C | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-2769_192-2767d others(5): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 106651451 | ||||||
| chr12:106651561 | A | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.192-2667A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106651561 | |||||||
| chr12:106651572 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.192-2656G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106651572 | |||||||
| chr12:106652154 | A | G | 2 | a0001c0002t0001g0135 a0001c0002t0005g0061 |
2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192-2074A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652154 | |||||||
| chr12:106652366 | G | A | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.192-1862G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652366 | |||||||
| chr12:106652428 | C | T | 62 | a0001c0001t0001g0149 a0001c0002t0001g0013 a0001c0002t0001g0014 others(59): Show |
62 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.192-1800C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652428 | |||||||
| chr12:106652442 | C | T | 88 | a0001c0001t0001g0149 a0001c0002t0001g0002 a0001c0002t0001g0013 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.192-1786C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652442 | |||||||
| chr12:106652607 | C | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.192-1621C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652607 | |||||||
| chr12:106652613 | C | T | 2 | a0001c0002t0001g0056 a0001c0002t0001g0057 |
2 | HG01168.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.192-1615C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652613 | |||||||
| chr12:106652807 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.192-1421C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652807 | |||||||
| chr12:106652925 | A | C | 1 | a0001c0002t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.192-1303A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652925 | |||||||
| chr12:106652945 | G | C | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.192-1283G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652945 | |||||||
| chr12:106652999 | T | G | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.192-1229T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106652999 | |||||||
| chr12:106653232 | T | C | 6 | a0001c0001t0001g0156 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG00639.hp2 HG01175.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-996T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106653232 | |||||||
| chr12:106653290 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.192-938C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106653290 | |||||||
| chr12:106653337 | G | C | 1 | a0001c0001t0001g0016 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.192-891G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106653337 | |||||||
| chr12:106653599 | G | A | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.192-629G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106653599 | |||||||
| chr12:106653600 | G | A | 2 | a0001c0002t0001g0135 a0001c0002t0005g0061 |
2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192-628G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106653600 | |||||||
| chr12:106653759 | C | T | 4 | a0001c0001t0001g0159 a0001c0001t0001g0207 a0001c0001t0001g0246 others(1): Show |
4 | NA18982.hp2 NA19054.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-469C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106653759 | |||||||
| chr12:106653888 | C | T | 14 | a0001c0003t0001g0009 a0001c0003t0001g0060 a0001c0003t0001g0072 others(11): Show |
14 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.192-340C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106653888 | |||||||
| chr12:106653958 | T | G | 1 | a0001c0001t0001g0288 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.192-270T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106653958 | |||||||
| chr12:106654137 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.192-91A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 3/17 | chr12 | 106654137 | |||||||
| chr12:106654554 | T | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+203T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106654554 | |||||||
| chr12:106654607 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.315+256C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106654607 | |||||||
| chr12:106654645 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+294G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106654645 | |||||||
| chr12:106654965 | GTCAATAC others(9): Show |
G | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+616_315+631del others(16): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106654965 | ||||||
| chr12:106654968 | A | C | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.315+617A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106654968 | |||||||
| chr12:106655230 | A | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.315+879A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106655230 | |||||||
| chr12:106655354 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.315+1003T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106655354 | |||||||
| chr12:106655493 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.315+1142C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106655493 | |||||||
| chr12:106655618 | C | T | 61 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.315+1267C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106655618 | |||||||
| chr12:106655641 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.315+1290C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106655641 | |||||||
| chr12:106655741 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.315+1390C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106655741 | |||||||
| chr12:106655772 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.315+1421C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106655772 | |||||||
| chr12:106655913 | T | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+1562T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106655913 | |||||||
| chr12:106655995 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.315+1644G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106655995 | |||||||
| chr12:106656094 | C | T | 10 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.315+1743C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106656094 | |||||||
| chr12:106656106 | T | C | 4 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+1755T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106656106 | |||||||
| chr12:106656349 | T | G | 1 | a0001c0002t0001g0191 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.315+1998T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106656349 | |||||||
| chr12:106656354 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.315+2003C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106656354 | |||||||
| chr12:106656392 | G | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.315+2041G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106656392 | |||||||
| chr12:106656393 | T | G | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.315+2042T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106656393 | |||||||
| chr12:106656510 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.315+2159C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106656510 | |||||||
| chr12:106656524 | C | T | 1 | a0001c0002t0001g0130 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.315+2173C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106656524 | |||||||
| chr12:106657082 | A | G | 5 | a0001c0003t0001g0060 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+2731A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106657082 | |||||||
| chr12:106657117 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.315+2766G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106657117 | |||||||
| chr12:106657386 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.315+3035C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106657386 | |||||||
| chr12:106657421 | C | T | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.315+3070C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106657421 | |||||||
| chr12:106657850 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.315+3499C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106657850 | |||||||
| chr12:106657868 | T | C | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.315+3517T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106657868 | |||||||
| chr12:106657900 | C | A | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.315+3549C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106657900 | |||||||
| chr12:106658049 | C | G | 55 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.315+3698C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658049 | |||||||
| chr12:106658062 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.315+3711C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658062 | |||||||
| chr12:106658264 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.315+3913C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658264 | |||||||
| chr12:106658444 | C | T | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+4093C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658444 | |||||||
| chr12:106658446 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.315+4095G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658446 | |||||||
| chr12:106658530 | T | C | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.315+4179T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658530 | |||||||
| chr12:106658616 | C | T | 51 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0031 others(48): Show |
51 | HG00438.hp1 HG00621.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.315+4265C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658616 | |||||||
| chr12:106658675 | T | C | 1 | a0001c0003t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.315+4324T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658675 | |||||||
| chr12:106658842 | G | A | 111 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0013 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.315+4491G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658842 | |||||||
| chr12:106658964 | C | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.315+4613C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106658964 | |||||||
| chr12:106659409 | A | G | 55 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.315+5058A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106659409 | |||||||
| chr12:106659577 | C | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.315+5226C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106659577 | |||||||
| chr12:106659768 | A | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.315+5417A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106659768 | |||||||
| chr12:106659828 | A | G | 55 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.315+5477A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106659828 | |||||||
| chr12:106659907 | C | T | 114 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0002 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.315+5556C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106659907 | |||||||
| chr12:106659984 | G | A | 3 | a0001c0002t0001g0165 a0001c0002t0001g0180 a0001c0002t0001g0185 |
3 | HG01256.hp2 HG03704.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.315+5633G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106659984 | |||||||
| chr12:106660020 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.315+5669T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106660020 | |||||||
| chr12:106660086 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01361.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+5735C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106660086 | |||||||
| chr12:106660329 | G | C | 1 | a0001c0002t0001g0015 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.315+5978G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106660329 | |||||||
| chr12:106660452 | C | T | 10 | a0001c0001t0001g0108 a0001c0001t0001g0276 a0001c0001t0001g0277 others(7): Show |
10 | HG01496.hp1 HG01943.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.315+6101C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106660452 | |||||||
| chr12:106660488 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.315+6137A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106660488 | |||||||
| chr12:106660704 | T | C | 17 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.315+6353T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106660704 | |||||||
| chr12:106660816 | A | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.315+6465A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106660816 | |||||||
| chr12:106660920 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.315+6569T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106660920 | |||||||
| chr12:106661244 | CT | C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.315+6897delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106661244 | ||||||
| chr12:106661471 | C | A | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.315+7120C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106661471 | |||||||
| chr12:106661625 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.315+7274G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106661625 | |||||||
| chr12:106661853 | T | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.315+7502T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106661853 | |||||||
| chr12:106661908 | G | C | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.315+7557G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106661908 | |||||||
| chr12:106661953 | T | A | 1 | a0001c0002t0001g0185 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.315+7602T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106661953 | |||||||
| chr12:106662103 | T | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+7752T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106662103 | |||||||
| chr12:106662111 | G | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+7760G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106662111 | |||||||
| chr12:106662556 | T | C | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+8205T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106662556 | |||||||
| chr12:106662596 | C | T | 1 | a0001c0004t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.315+8245C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106662596 | |||||||
| chr12:106662765 | C | CT | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+8421dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106662765 | ||||||
| chr12:106662816 | A | G | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.315+8465A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106662816 | |||||||
| chr12:106662867 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.315+8516C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106662867 | |||||||
| chr12:106662875 | A | G | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.315+8524A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106662875 | |||||||
| chr12:106663279 | G | A | 1 | a0001c0002t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.315+8928G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106663279 | |||||||
| chr12:106663345 | G | A | 2 | a0001c0002t0001g0237 a0001c0002t0001g0275 |
2 | NA18959.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.315+8994G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106663345 | |||||||
| chr12:106663756 | G | GT | 7 | a0001c0001t0001g0196 a0001c0001t0001g0217 a0001c0002t0001g0068 others(4): Show |
7 | HG01109.hp1 HG01192.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.315+9417dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106663756 | ||||||
| chr12:106663814 | T | A | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.315+9463T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106663814 | |||||||
| chr12:106664094 | C | G | 1 | a0001c0001t0001g0266 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.315+9743C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106664094 | |||||||
| chr12:106664259 | G | A | 54 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.315+9908G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106664259 | |||||||
| chr12:106664267 | C | T | 221 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(218): Show |
221 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.315+9916C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106664267 | |||||||
| chr12:106664618 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0267 |
2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.315+10267C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106664618 | |||||||
| chr12:106664664 | C | A | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.315+10313C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106664664 | |||||||
| chr12:106664852 | C | A | 55 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.315+10501C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106664852 | |||||||
| chr12:106665011 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.315+10660G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665011 | |||||||
| chr12:106665097 | A | T | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.315+10746A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665097 | |||||||
| chr12:106665210 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.315+10859G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665210 | |||||||
| chr12:106665301 | T | C | 58 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.315+10950T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665301 | |||||||
| chr12:106665318 | G | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.315+10967G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665318 | |||||||
| chr12:106665480 | C | T | 1 | a0001c0002t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.315+11129C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665480 | |||||||
| chr12:106665484 | G | A | 55 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0031 others(52): Show |
55 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.315+11133G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665484 | |||||||
| chr12:106665520 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.315+11169T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665520 | |||||||
| chr12:106665605 | T | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01361.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+11254T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665605 | |||||||
| chr12:106665667 | A | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG00621.hp2 HG03492.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.315+11316A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665667 | |||||||
| chr12:106665816 | AC | A | 50 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.315+11466delC | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106665816 | |||||||
| chr12:106666021 | C | T | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+11670C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666021 | |||||||
| chr12:106666159 | A | G | 1 | a0001c0003t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.315+11808A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666159 | |||||||
| chr12:106666161 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.315+11810G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666161 | |||||||
| chr12:106666317 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+11966G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666317 | |||||||
| chr12:106666373 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.315+12022G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666373 | |||||||
| chr12:106666492 | A | G | 7 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.315+12141A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666492 | |||||||
| chr12:106666594 | C | T | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.315+12243C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666594 | |||||||
| chr12:106666677 | G | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.315+12326G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666677 | |||||||
| chr12:106666735 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.315+12384G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666735 | |||||||
| chr12:106666860 | T | A | 56 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0002 others(53): Show |
56 | HG00438.hp1 HG00621.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.315+12509T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106666860 | |||||||
| chr12:106667044 | G | A | 1 | a0001c0002t0001g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+12693G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106667044 | |||||||
| chr12:106667079 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.315+12728A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106667079 | |||||||
| chr12:106667235 | G | C | 6 | a0001c0003t0001g0019 a0001c0003t0001g0060 a0001c0003t0001g0109 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+12884G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106667235 | |||||||
| chr12:106667370 | G | T | 1 | a0001c0002t0001g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.315+13019G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106667370 | |||||||
| chr12:106667597 | A | G | 45 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0035 others(42): Show |
45 | HG00408.hp1 HG00438.hp2 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.315+13246A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106667597 | |||||||
| chr12:106667670 | C | T | 15 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0060 others(12): Show |
15 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.315+13319C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106667670 | |||||||
| chr12:106668005 | C | T | 54 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.315+13654C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668005 | |||||||
| chr12:106668024 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.315+13673G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668024 | |||||||
| chr12:106668108 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.315+13757G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668108 | |||||||
| chr12:106668270 | G | GA | 7 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.316-13716dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106668270 | ||||||
| chr12:106668345 | C | A | 1 | a0001c0002t0001g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.316-13648C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668345 | |||||||
| chr12:106668468 | C | T | 114 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0002 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.316-13525C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668468 | |||||||
| chr12:106668551 | C | T | 114 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0002 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.316-13442C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668551 | |||||||
| chr12:106668571 | A | T | 5 | a0001c0001t0001g0194 a0001c0001t0001g0245 a0001c0002t0001g0017 others(2): Show |
5 | HG00741.hp2 HG02698.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.316-13422A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668571 | |||||||
| chr12:106668677 | GC | G | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-13314delC | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106668677 | ||||||
| chr12:106668696 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.316-13297G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668696 | |||||||
| chr12:106668819 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.316-13174A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668819 | |||||||
| chr12:106668850 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.316-13143T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668850 | |||||||
| chr12:106668889 | G | A | 2 | a0001c0003t0001g0060 a0001c0003t0001g0228 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.316-13104G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668889 | |||||||
| chr12:106668890 | G | A | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.316-13103G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668890 | |||||||
| chr12:106668978 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.316-13015G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106668978 | |||||||
| chr12:106669395 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.316-12598G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106669395 | |||||||
| chr12:106669439 | C | T | 1 | a0001c0002t0001g0162 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.316-12554C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106669439 | |||||||
| chr12:106669562 | C | A | 110 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0002t0001g0013 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-12431C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106669562 | |||||||
| chr12:106669707 | G | GA | 58 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.316-12277dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669707 | ||||||
| chr12:106669720 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG02615.hp1 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.316-12273G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106669720 | |||||||
| chr12:106669837 | G | GGT | 12 | a0001c0002t0001g0020 a0001c0002t0001g0124 a0001c0002t0001g0155 others(9): Show |
12 | HG00099.hp2 HG01175.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.316-12155_316-1215 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669837 | ||||||
| chr12:106669837 | G | GGTGT | 25 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(22): Show |
25 | HG00639.hp2 HG00735.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.316-12155_316-1215 others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669837 | ||||||
| chr12:106669837 | G | GGTGTGT | 22 | a0001c0001t0001g0166 a0001c0002t0001g0018 a0001c0002t0001g0037 others(19): Show |
22 | HG00621.hp1 HG00639.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.316-12155_316-1215 others(10): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669837 | ||||||
| chr12:106669837 | G | GGTGTGTG others(1): Show |
38 | a0001c0002t0001g0021 a0001c0002t0001g0029 a0001c0002t0001g0032 others(35): Show |
38 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.316-12155_316-1215 others(12): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669837 | ||||||
| chr12:106669837 | G | GGTGTGTG others(3): Show |
7 | a0001c0001t0001g0167 a0001c0002t0001g0045 a0001c0002t0001g0048 others(4): Show |
7 | HG00738.hp2 HG01934.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-12155_316-1215 others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669837 | ||||||
| chr12:106669837 | G | GGTGTGTG others(5): Show |
1 | a0001c0002t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.316-12155_316-1215 others(16): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669837 | ||||||
| chr12:106669837 | G | GGTGTGTG others(9): Show |
1 | a0001c0002t0001g0134 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.316-12155_316-1215 others(20): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669837 | ||||||
| chr12:106669839 | G | GGT | 27 | a0001c0001t0001g0084 a0001c0001t0001g0131 a0001c0001t0001g0156 others(24): Show |
27 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.316-12115_316-1211 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669839 | ||||||
| chr12:106669839 | G | GGTGT | 6 | a0001c0001t0001g0118 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG01256.hp1 HG01258.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-12117_316-1211 others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669839 | ||||||
| chr12:106669839 | G | GGTGTGT | 7 | a0001c0001t0001g0003 a0001c0001t0001g0236 a0001c0001t0001g0263 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.316-12119_316-1211 others(10): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669839 | ||||||
| chr12:106669839 | G | GGTGTGTG others(1): Show |
7 | a0001c0001t0001g0210 a0001c0002t0001g0002 a0001c0002t0001g0063 others(4): Show |
7 | HG02027.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-12121_316-1211 others(12): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669839 | ||||||
| chr12:106669839 | G | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0166 a0001c0001t0001g0167 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.316-12154G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106669839 | |||||||
| chr12:106669839 | GGT | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
82 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.316-12115_316-1211 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669839 | ||||||
| chr12:106669839 | GGTGT | G | 4 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG02615.hp1 HG02738.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-12117_316-1211 others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669839 | ||||||
| chr12:106669839 | GGTGTGTG others(3): Show |
G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01496.hp1 HG01943.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.316-12123_316-1211 others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106669839 | ||||||
| chr12:106669841 | T | G | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.316-12152T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106669841 | |||||||
| chr12:106669843 | T | G | 2 | a0001c0001t0001g0256 a0001c0002t0001g0239 |
2 | NA19004.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.316-12150T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106669843 | |||||||
| chr12:106670310 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.316-11683C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106670310 | |||||||
| chr12:106670402 | T | C | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.316-11591T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106670402 | |||||||
| chr12:106670629 | C | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.316-11364C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106670629 | |||||||
| chr12:106670964 | ATGTG | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-11025_316-1102 others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106670964 | ||||||
| chr12:106671125 | A | G | 4 | a0001c0001t0001g0087 a0001c0001t0001g0103 a0001c0001t0001g0105 others(1): Show |
4 | HG03041.hp1 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-10868A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106671125 | |||||||
| chr12:106671402 | T | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(4): Show |
7 | HG01361.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-10591T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106671402 | |||||||
| chr12:106671480 | A | G | 114 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.316-10513A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106671480 | |||||||
| chr12:106671600 | T | A | 52 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(49): Show |
52 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.316-10393T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106671600 | |||||||
| chr12:106672219 | T | C | 1 | a0001c0002t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.316-9774T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106672219 | |||||||
| chr12:106672292 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-9701G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106672292 | |||||||
| chr12:106672390 | G | A | 2 | a0001c0002t0001g0018 a0001c0002t0001g0020 |
2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.316-9603G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106672390 | |||||||
| chr12:106672518 | C | T | 17 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.316-9475C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106672518 | |||||||
| chr12:106672633 | C | T | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.316-9360C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106672633 | |||||||
| chr12:106672763 | T | TA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
69 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.316-9213dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106672763 | ||||||
| chr12:106672763 | T | TAA | 21 | a0001c0002t0001g0002 a0001c0002t0001g0017 a0001c0002t0001g0018 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.316-9214_316-9213d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106672763 | ||||||
| chr12:106672763 | TA | T | 19 | a0001c0001t0001g0106 a0001c0002t0001g0013 a0001c0002t0001g0053 others(16): Show |
19 | HG01175.hp1 HG01952.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.316-9213delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106672763 | ||||||
| chr12:106673210 | A | G | 54 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.316-8783A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106673210 | |||||||
| chr12:106673280 | C | A | 2 | a0001c0002t0001g0272 a0001c0002t0001g0273 |
2 | HG02135.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.316-8713C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106673280 | |||||||
| chr12:106673382 | C | T | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.316-8611C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106673382 | |||||||
| chr12:106673400 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.316-8593G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106673400 | |||||||
| chr12:106673784 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.316-8209A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106673784 | |||||||
| chr12:106674163 | A | T | 2 | a0001c0003t0001g0141 a0001c0003t0001g0143 |
2 | HG01109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.316-7830A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106674163 | |||||||
| chr12:106674300 | T | C | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-7693T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106674300 | |||||||
| chr12:106674609 | C | T | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.316-7384C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106674609 | |||||||
| chr12:106674886 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-7107A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106674886 | |||||||
| chr12:106675028 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.316-6965G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106675028 | |||||||
| chr12:106675130 | C | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316-6863C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106675130 | |||||||
| chr12:106675159 | C | T | 1 | a0001c0002t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.316-6834C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106675159 | |||||||
| chr12:106675325 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.316-6668G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106675325 | |||||||
| chr12:106675527 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.316-6466G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106675527 | |||||||
| chr12:106675554 | A | C | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.316-6439A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106675554 | |||||||
| chr12:106676055 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.316-5938G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106676055 | |||||||
| chr12:106676208 | G | A | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.316-5785G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106676208 | |||||||
| chr12:106676220 | C | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0203 |
2 | HG00735.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.316-5773C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106676220 | |||||||
| chr12:106676264 | G | C | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.316-5729G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106676264 | |||||||
| chr12:106676271 | T | G | 112 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.316-5722T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106676271 | |||||||
| chr12:106676533 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-5460A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106676533 | |||||||
| chr12:106676647 | A | T | 129 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.316-5346A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106676647 | |||||||
| chr12:106676797 | C | T | 58 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.316-5196C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106676797 | |||||||
| chr12:106676853 | T | C | 2 | a0001c0002t0001g0049 a0001c0002t0001g0083 |
2 | HG00609.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.316-5140T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106676853 | |||||||
| chr12:106677095 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.316-4898C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677095 | |||||||
| chr12:106677149 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.316-4844C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677149 | |||||||
| chr12:106677215 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.316-4778G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677215 | |||||||
| chr12:106677272 | A | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0035 others(34): Show |
37 | HG00408.hp1 HG00438.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.316-4721A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677272 | |||||||
| chr12:106677352 | C | T | 110 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-4641C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677352 | |||||||
| chr12:106677355 | T | C | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316-4638T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677355 | |||||||
| chr12:106677404 | C | T | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.316-4589C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677404 | |||||||
| chr12:106677463 | C | A | 1 | a0001c0002t0001g0239 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.316-4530C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677463 | |||||||
| chr12:106677820 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.316-4173C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677820 | |||||||
| chr12:106677823 | T | C | 1 | a0001c0002t0001g0059 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.316-4170T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677823 | |||||||
| chr12:106677825 | G | A | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316-4168G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677825 | |||||||
| chr12:106677834 | A | G | 1 | a0001c0002t0001g0258 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.316-4159A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677834 | |||||||
| chr12:106677859 | G | A | 49 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(46): Show |
49 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.316-4134G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677859 | |||||||
| chr12:106677877 | A | G | 10 | a0001c0002t0001g0034 a0001c0002t0001g0038 a0001c0002t0001g0039 others(7): Show |
10 | HG00408.hp2 HG00609.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.316-4116A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106677877 | |||||||
| chr12:106678022 | T | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.316-3971T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678022 | |||||||
| chr12:106678049 | G | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.316-3944G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678049 | |||||||
| chr12:106678064 | T | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.316-3929T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678064 | |||||||
| chr12:106678097 | A | G | 1 | a0001c0002t0001g0140 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.316-3896A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678097 | |||||||
| chr12:106678133 | G | A | 49 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(46): Show |
49 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.316-3860G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678133 | |||||||
| chr12:106678314 | T | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-3679T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678314 | |||||||
| chr12:106678509 | A | G | 1 | a0004c0008t0001g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.316-3484A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678509 | |||||||
| chr12:106678836 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.316-3157G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678836 | |||||||
| chr12:106678949 | T | C | 1 | a0001c0002t0001g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.316-3044T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678949 | |||||||
| chr12:106678991 | G | T | 4 | a0001c0002t0001g0059 a0001c0002t0001g0157 a0001c0002t0001g0179 others(1): Show |
4 | HG01167.hp1 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-3002G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106678991 | |||||||
| chr12:106679193 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.316-2800C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679193 | |||||||
| chr12:106679303 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.316-2690C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679303 | |||||||
| chr12:106679327 | C | T | 6 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0001g0187 others(3): Show |
6 | HG00438.hp1 HG00621.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-2666C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679327 | |||||||
| chr12:106679457 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.316-2536A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679457 | |||||||
| chr12:106679464 | CA | C | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.316-2518delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 106679464 | ||||||
| chr12:106679474 | A | C | 1 | a0001c0003t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316-2519A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679474 | |||||||
| chr12:106679475 | A | C | 53 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(50): Show |
53 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.316-2518A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679475 | |||||||
| chr12:106679538 | C | A | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.316-2455C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679538 | |||||||
| chr12:106679565 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.316-2428C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679565 | |||||||
| chr12:106679718 | G | A | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.316-2275G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679718 | |||||||
| chr12:106679790 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.316-2203C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106679790 | |||||||
| chr12:106680049 | C | T | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-1944C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106680049 | |||||||
| chr12:106680269 | T | C | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-1724T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106680269 | |||||||
| chr12:106680632 | T | A | 110 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-1361T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106680632 | |||||||
| chr12:106680752 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.316-1241A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106680752 | |||||||
| chr12:106680773 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0055 |
3 | HG02622.hp1 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316-1220A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106680773 | |||||||
| chr12:106680803 | C | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316-1190C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106680803 | |||||||
| chr12:106681225 | T | C | 1 | a0001c0002t0001g0258 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.316-768T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106681225 | |||||||
| chr12:106681267 | C | T | 4 | a0001c0002t0001g0155 a0001c0002t0001g0272 a0001c0002t0001g0273 others(1): Show |
4 | HG02135.hp2 NA18747.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-726C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106681267 | |||||||
| chr12:106681335 | A | G | 2 | a0001c0002t0001g0033 a0001c0002t0001g0050 |
2 | HG02155.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.316-658A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106681335 | |||||||
| chr12:106681392 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.316-601T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106681392 | |||||||
| chr12:106681432 | C | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
89 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.316-561C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106681432 | |||||||
| chr12:106681705 | G | T | 1 | a0001c0002t0001g0235 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.316-288G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106681705 | |||||||
| chr12:106681732 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.316-261C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106681732 | |||||||
| chr12:106681755 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.316-238C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106681755 | |||||||
| chr12:106681756 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.316-237G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 4/17 | chr12 | 106681756 | |||||||
| chr12:106682096 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.377+42A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106682096 | |||||||
| chr12:106682125 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.377+71C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106682125 | |||||||
| chr12:106682545 | C | A | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.377+491C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106682545 | |||||||
| chr12:106682627 | A | G | 114 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.377+573A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106682627 | |||||||
| chr12:106682999 | T | C | 4 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+945T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106682999 | |||||||
| chr12:106683205 | G | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.377+1151G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683205 | |||||||
| chr12:106683335 | AAAT | A | 54 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.377+1285_377+1287d others(5): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683335 | ||||||
| chr12:106683394 | A | G | 111 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.377+1340A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683394 | |||||||
| chr12:106683401 | A | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
89 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.377+1347A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683401 | |||||||
| chr12:106683454 | G | A | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.377+1400G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683454 | |||||||
| chr12:106683466 | G | GA | 13 | a0001c0001t0001g0028 a0001c0001t0001g0094 a0001c0001t0001g0104 others(10): Show |
13 | HG01074.hp2 HG01258.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.377+1442dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683466 | ||||||
| chr12:106683466 | G | GAA | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(82): Show |
85 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.377+1441_377+1442d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683466 | ||||||
| chr12:106683466 | G | GAAA | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(36): Show |
39 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.377+1440_377+1442d others(5): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683466 | ||||||
| chr12:106683466 | G | GAAAA | 18 | a0001c0001t0001g0091 a0001c0001t0001g0097 a0001c0001t0001g0107 others(15): Show |
18 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.377+1439_377+1442d others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683466 | ||||||
| chr12:106683466 | GA | G | 37 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0243 others(34): Show |
37 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.377+1442delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683466 | ||||||
| chr12:106683466 | GAA | G | 10 | a0001c0002t0001g0029 a0001c0002t0001g0125 a0001c0002t0001g0126 others(7): Show |
10 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.377+1441_377+1442d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683466 | ||||||
| chr12:106683466 | GAAA | G | 59 | a0001c0001t0001g0230 a0001c0001t0001g0232 a0001c0002t0001g0017 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.377+1440_377+1442d others(5): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683466 | ||||||
| chr12:106683466 | GAAAA | G | 9 | a0001c0002t0001g0120 a0001c0002t0001g0162 a0001c0002t0001g0171 others(6): Show |
9 | HG01943.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.377+1439_377+1442d others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683466 | ||||||
| chr12:106683466 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.377+1433_377+1442d others(12): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106683466 | ||||||
| chr12:106683476 | A | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.377+1422A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683476 | |||||||
| chr12:106683478 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.377+1424A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683478 | |||||||
| chr12:106683480 | A | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.377+1426A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683480 | |||||||
| chr12:106683481 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.377+1427A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683481 | |||||||
| chr12:106683484 | A | C | 2 | a0001c0002t0001g0002 a0001c0002t0001g0135 |
2 | HG02027.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.377+1430A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683484 | |||||||
| chr12:106683486 | A | C | 1 | a0001c0003t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.377+1432A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683486 | |||||||
| chr12:106683489 | A | C | 1 | a0001c0002t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.377+1435A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683489 | |||||||
| chr12:106683493 | A | C | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.377+1439A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683493 | |||||||
| chr12:106683545 | G | T | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.377+1491G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683545 | |||||||
| chr12:106683654 | T | C | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.377+1600T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683654 | |||||||
| chr12:106683726 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.377+1672G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683726 | |||||||
| chr12:106683737 | G | A | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.377+1683G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683737 | |||||||
| chr12:106683885 | T | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377+1831T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106683885 | |||||||
| chr12:106684147 | A | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.377+2093A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106684147 | |||||||
| chr12:106684393 | C | A | 1 | a0001c0002t0001g0237 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.377+2339C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106684393 | |||||||
| chr12:106684670 | C | T | 110 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.378-2214C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106684670 | |||||||
| chr12:106684784 | A | AAAG | 222 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
222 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.378-2097_378-2095d others(5): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106684784 | ||||||
| chr12:106685073 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.378-1811C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106685073 | |||||||
| chr12:106685171 | G | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.378-1713G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106685171 | |||||||
| chr12:106685448 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.378-1436C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106685448 | |||||||
| chr12:106685512 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.378-1372C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106685512 | |||||||
| chr12:106685517 | T | G | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.378-1367T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106685517 | |||||||
| chr12:106685719 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.378-1165G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106685719 | |||||||
| chr12:106686139 | G | A | 7 | a0001c0001t0001g0177 a0001c0002t0001g0053 a0001c0003t0001g0009 others(4): Show |
7 | HG01175.hp1 HG01952.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-745G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106686139 | |||||||
| chr12:106686216 | A | G | 112 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.378-668A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106686216 | |||||||
| chr12:106686260 | T | C | 113 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.378-624T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106686260 | |||||||
| chr12:106686349 | G | T | 50 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(47): Show |
50 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.378-535G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106686349 | |||||||
| chr12:106686411 | C | CA | 6 | a0001c0001t0001g0282 a0001c0002t0001g0002 a0001c0002t0001g0127 others(3): Show |
6 | HG02027.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378-458dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106686411 | ||||||
| chr12:106686457 | C | T | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.378-427C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106686457 | |||||||
| chr12:106686535 | C | A | 112 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.378-349C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106686535 | |||||||
| chr12:106686653 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.378-231T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106686653 | |||||||
| chr12:106686839 | CT | C | 20 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(17): Show |
20 | HG01168.hp1 HG01169.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.378-32delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106686839 | ||||||
| chr12:106686848 | TTTTTC | T | 96 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(93): Show |
96 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.378-34_378-30delTT others(3): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106686848 | ||||||
| chr12:106686849 | TTTTC | T | 13 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.378-33_378-30delTT others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 106686849 | ||||||
| chr12:106686851 | T | C | 2 | a0001c0002t0001g0002 a0001c0002t0001g0058 |
2 | HG02027.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.378-33T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106686851 | |||||||
| chr12:106686862 | C | T | 110 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.378-22C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 5/17 | chr12 | 106686862 | |||||||
| chr12:106687167 | A | ATC | 28 | a0001c0002t0001g0021 a0001c0002t0001g0041 a0001c0002t0001g0042 others(25): Show |
28 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.591+85_591+86dupTC | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687167 | ||||||
| chr12:106687167 | A | ATCTC | 15 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0029 others(12): Show |
15 | HG00099.hp2 HG01081.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+83_591+86dupTC others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687167 | ||||||
| chr12:106687180 | TCTCA | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0123 |
4 | HG03139.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+85_591+88delTC others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687180 | ||||||
| chr12:106687180 | TCTCACAC others(3): Show |
T | 1 | a0001c0001t0001g0007 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.591+85_591+94delTC others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687180 | ||||||
| chr12:106687182 | T | TCA | 4 | a0001c0001t0001g0003 a0001c0001t0001g0178 a0001c0001t0001g0266 others(1): Show |
4 | HG01099.hp2 NA18964.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+128_591+129dup others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | T | TCTCA | 9 | a0001c0002t0001g0155 a0001c0002t0001g0215 a0001c0002t0001g0229 others(6): Show |
9 | HG02135.hp2 HG02683.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.591+86_591+87insTC others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | T | TCTCACA | 6 | a0001c0002t0001g0059 a0001c0002t0001g0136 a0001c0002t0001g0138 others(3): Show |
6 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.591+86_591+87insTC others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | T | TCTCACAC others(3): Show |
1 | a0001c0003t0001g0074 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.591+86_591+87insTC others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | T | TCTCACAC others(5): Show |
1 | a0001c0003t0001g0072 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.591+86_591+87insTC others(10): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | T | TCTCTCA | 7 | a0001c0002t0001g0032 a0001c0002t0001g0050 a0001c0002t0001g0119 others(4): Show |
7 | HG01074.hp1 HG01109.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.591+86_591+87insTC others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | T | TCTCTCAC others(3): Show |
2 | a0001c0003t0001g0009 a0001c0003t0001g0144 |
2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.591+86_591+87insTC others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | T | TCTCTCAC others(5): Show |
1 | a0001c0002t0001g0018 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.591+86_591+87insTC others(10): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | TCA | T | 10 | a0001c0001t0001g0156 a0001c0001t0001g0164 a0001c0001t0001g0198 others(7): Show |
10 | HG01069.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.591+128_591+129del others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | TCACA | T | 48 | a0001c0001t0001g0084 a0001c0001t0001g0154 a0001c0001t0001g0158 others(45): Show |
48 | HG00140.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.591+126_591+129del others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | TCACACA | T | 18 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0001c0001t0001g0199 others(15): Show |
18 | HG01361.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.591+124_591+129del others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | TCACACAC others(1): Show |
T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0093 others(19): Show |
22 | HG00099.hp1 HG01123.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.591+122_591+129del others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | TCACACAC others(3): Show |
T | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(79): Show |
82 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.591+120_591+129del others(10): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687182 | TCACACAC others(5): Show |
T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02257.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.591+118_591+129del others(12): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687182 | ||||||
| chr12:106687184 | A | T | 42 | a0001c0002t0001g0021 a0001c0002t0001g0031 a0001c0002t0001g0034 others(39): Show |
42 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.591+87A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687184 | |||||||
| chr12:106687186 | A | T | 23 | a0001c0002t0001g0034 a0001c0002t0001g0038 a0001c0002t0001g0039 others(20): Show |
23 | HG00408.hp2 HG00609.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.591+89A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687186 | |||||||
| chr12:106687188 | A | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0002t0001g0002 others(1): Show |
4 | HG02027.hp1 HG02027.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+91A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687188 | |||||||
| chr12:106687190 | A | T | 11 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0001g0289 others(8): Show |
11 | HG02027.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.591+93A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687190 | |||||||
| chr12:106687192 | A | T | 10 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(7): Show |
10 | HG01123.hp2 HG01433.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.591+95A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687192 | |||||||
| chr12:106687194 | A | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0035 others(40): Show |
43 | HG00408.hp1 HG00438.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.591+97A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687194 | |||||||
| chr12:106687196 | A | T | 11 | a0001c0001t0001g0035 a0001c0001t0001g0104 a0001c0001t0004g0036 others(8): Show |
11 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.591+99A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687196 | |||||||
| chr12:106687198 | A | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.591+101A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687198 | |||||||
| chr12:106687269 | C | T | 1 | a0001c0002t0001g0174 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.591+172C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687269 | |||||||
| chr12:106687486 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.591+389T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687486 | |||||||
| chr12:106687536 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.591+439C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687536 | |||||||
| chr12:106687549 | C | CAAAAAAA others(6): Show |
1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.591+456_591+468dup others(13): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687549 | ||||||
| chr12:106687549 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.591+454_591+468dup others(15): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687549 | ||||||
| chr12:106687549 | CA | C | 38 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(35): Show |
38 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.591+468delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106687549 | ||||||
| chr12:106687821 | C | A | 130 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.591+724C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106687821 | |||||||
| chr12:106688064 | C | CT | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(35): Show |
38 | HG00735.hp2 HG00741.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.591+990dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106688064 | ||||||
| chr12:106688064 | CT | C | 8 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
8 | NA18948.hp1 NA18966.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.591+990delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106688064 | ||||||
| chr12:106688072 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.591+975T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688072 | |||||||
| chr12:106688131 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.591+1034G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688131 | |||||||
| chr12:106688131 | G | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.591+1034G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688131 | |||||||
| chr12:106688143 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.591+1046C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688143 | |||||||
| chr12:106688414 | C | G | 1 | a0001c0001t0001g0266 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.592-873C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688414 | |||||||
| chr12:106688424 | T | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.592-863T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688424 | |||||||
| chr12:106688537 | G | A | 10 | a0001c0001t0001g0108 a0001c0001t0001g0276 a0001c0001t0001g0277 others(7): Show |
10 | HG01496.hp1 HG01943.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-750G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688537 | |||||||
| chr12:106688677 | A | G | 112 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.592-610A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688677 | |||||||
| chr12:106688718 | G | T | 130 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.592-569G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688718 | |||||||
| chr12:106688769 | AT | A | 117 | a0001c0001t0001g0080 a0001c0001t0001g0111 a0001c0001t0001g0148 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.592-507delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 106688769 | ||||||
| chr12:106688774 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.592-513T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688774 | |||||||
| chr12:106688822 | T | C | 1 | a0001c0002t0001g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.592-465T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106688822 | |||||||
| chr12:106689013 | G | C | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.592-274G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106689013 | |||||||
| chr12:106689047 | G | A | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG01943.hp2 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-240G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106689047 | |||||||
| chr12:106689077 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.592-210G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106689077 | |||||||
| chr12:106689253 | G | A | 109 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.592-34G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106689253 | |||||||
| chr12:106689269 | C | G | 1 | a0001c0002t0001g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.592-18C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106689269 | |||||||
| chr12:106689281 | C | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
89 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(86): Show |
splice_region_variant&intron_variant | LOW | c.592-6C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 6/17 | chr12 | 106689281 | |||||||
| chr12:106689432 | A | T | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.669+68A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106689432 | |||||||
| chr12:106689454 | G | C | 1 | a0001c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.669+90G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106689454 | |||||||
| chr12:106689527 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.669+163C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106689527 | |||||||
| chr12:106690018 | T | C | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.669+654T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690018 | |||||||
| chr12:106690050 | C | T | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.669+686C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690050 | |||||||
| chr12:106690104 | A | G | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.669+740A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690104 | |||||||
| chr12:106690118 | G | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0245 |
2 | HG00741.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.669+754G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690118 | |||||||
| chr12:106690298 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02257.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.669+934A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690298 | |||||||
| chr12:106690327 | C | T | 1 | a0001c0002t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.669+963C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690327 | |||||||
| chr12:106690401 | G | A | 49 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.669+1037G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690401 | |||||||
| chr12:106690517 | G | A | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+1153G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690517 | |||||||
| chr12:106690581 | T | TG | 57 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(54): Show |
57 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.669+1223dupG | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 106690581 | ||||||
| chr12:106690604 | G | C | 54 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.669+1240G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690604 | |||||||
| chr12:106690745 | C | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.669+1381C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690745 | |||||||
| chr12:106690829 | A | G | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+1465A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690829 | |||||||
| chr12:106690968 | A | G | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.669+1604A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690968 | |||||||
| chr12:106690993 | G | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.669+1629G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106690993 | |||||||
| chr12:106691010 | T | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.669+1646T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691010 | |||||||
| chr12:106691019 | G | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.669+1655G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691019 | |||||||
| chr12:106691048 | A | G | 10 | a0001c0002t0001g0034 a0001c0002t0001g0038 a0001c0002t0001g0039 others(7): Show |
10 | HG00408.hp2 HG00609.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.669+1684A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691048 | |||||||
| chr12:106691058 | T | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.669+1694T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691058 | |||||||
| chr12:106691088 | C | A | 1 | a0001c0001t0001g0030 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.669+1724C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691088 | |||||||
| chr12:106691236 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.669+1872G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691236 | |||||||
| chr12:106691287 | T | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.669+1923T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691287 | |||||||
| chr12:106691393 | C | G | 125 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(122): Show |
125 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.669+2029C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691393 | |||||||
| chr12:106691449 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.669+2085G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691449 | |||||||
| chr12:106691504 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.669+2140G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691504 | |||||||
| chr12:106691632 | A | T | 1 | a0001c0001t0001g0008 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.669+2268A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691632 | |||||||
| chr12:106691680 | G | A | 1 | a0001c0002t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.669+2316G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691680 | |||||||
| chr12:106691922 | G | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+2558G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106691922 | |||||||
| chr12:106692011 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.669+2647G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106692011 | |||||||
| chr12:106692057 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.669+2693C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106692057 | |||||||
| chr12:106692155 | C | CA | 12 | a0001c0001t0001g0114 a0001c0001t0004g0036 a0001c0002t0001g0002 others(9): Show |
12 | HG02027.hp1 HG02109.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.669+2808dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 106692155 | ||||||
| chr12:106692173 | T | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.669+2809T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106692173 | |||||||
| chr12:106692462 | G | T | 112 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.669+3098G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106692462 | |||||||
| chr12:106692467 | G | T | 112 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.669+3103G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106692467 | |||||||
| chr12:106692485 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.669+3121A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106692485 | |||||||
| chr12:106692591 | C | T | 50 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(47): Show |
50 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.669+3227C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106692591 | |||||||
| chr12:106692596 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.669+3232C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106692596 | |||||||
| chr12:106692835 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.670-3448T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106692835 | |||||||
| chr12:106693094 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.670-3189T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693094 | |||||||
| chr12:106693213 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.670-3070T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693213 | |||||||
| chr12:106693216 | T | C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.670-3067T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693216 | |||||||
| chr12:106693463 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.670-2820G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693463 | |||||||
| chr12:106693594 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0245 |
2 | HG00741.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.670-2689T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693594 | |||||||
| chr12:106693623 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG01258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.670-2660C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693623 | |||||||
| chr12:106693654 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.670-2629T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693654 | |||||||
| chr12:106693690 | C | T | 6 | a0001c0003t0001g0019 a0001c0003t0001g0060 a0001c0003t0001g0109 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-2593C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693690 | |||||||
| chr12:106693748 | G | A | 21 | a0001c0001t0001g0088 a0001c0002t0001g0017 a0001c0002t0001g0018 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.670-2535G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693748 | |||||||
| chr12:106693761 | G | A | 1 | a0001c0002t0001g0042 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.670-2522G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693761 | |||||||
| chr12:106693856 | T | A | 1 | a0001c0001t0001g0292 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.670-2427T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106693856 | |||||||
| chr12:106694107 | T | C | 1 | a0001c0003t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.670-2176T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106694107 | |||||||
| chr12:106694383 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.670-1900T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106694383 | |||||||
| chr12:106694429 | G | A | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.670-1854G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106694429 | |||||||
| chr12:106694611 | A | T | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.670-1672A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106694611 | |||||||
| chr12:106694719 | C | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.670-1564C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106694719 | |||||||
| chr12:106694793 | G | C | 1 | a0001c0003t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.670-1490G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106694793 | |||||||
| chr12:106694802 | A | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0286 a0001c0001t0001g0293 |
3 | HG03834.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.670-1481A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106694802 | |||||||
| chr12:106694803 | G | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-1480G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106694803 | |||||||
| chr12:106694860 | C | A | 6 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0001g0187 others(3): Show |
6 | HG00438.hp1 HG00621.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-1423C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106694860 | |||||||
| chr12:106695058 | C | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.670-1225C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106695058 | |||||||
| chr12:106695188 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.670-1095G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106695188 | |||||||
| chr12:106695245 | C | CAG | 115 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.670-1037_670-1036d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 106695245 | ||||||
| chr12:106695352 | A | G | 2 | a0001c0002t0001g0013 a0001c0002t0001g0014 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.670-931A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106695352 | |||||||
| chr12:106695409 | C | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18964.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.670-874C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106695409 | |||||||
| chr12:106695647 | A | C | 1 | a0001c0002t0001g0133 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.670-636A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106695647 | |||||||
| chr12:106695780 | A | T | 1 | a0001c0002t0001g0215 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.670-503A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106695780 | |||||||
| chr12:106695830 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.670-453T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106695830 | |||||||
| chr12:106695870 | T | C | 2 | a0001c0002t0001g0135 a0001c0002t0006g0147 |
2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.670-413T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106695870 | |||||||
| chr12:106696028 | GC | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0086 others(11): Show |
14 | HG00408.hp1 HG00438.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-254delC | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106696028 | |||||||
| chr12:106696079 | G | T | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.670-204G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106696079 | |||||||
| chr12:106696156 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.670-127G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 7/17 | chr12 | 106696156 | |||||||
| chr12:106696795 | AT | A | 54 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.833+350delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106696795 | |||||||
| chr12:106696838 | C | T | 113 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.833+392C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106696838 | |||||||
| chr12:106697170 | G | A | 1 | a0001c0002t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.833+724G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106697170 | |||||||
| chr12:106697445 | C | CT | 26 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(23): Show |
26 | HG00621.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.833+1013dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106697445 | ||||||
| chr12:106697445 | C | CTT | 108 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(105): Show |
108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.833+1012_833+1013d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106697445 | ||||||
| chr12:106697613 | C | G | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.833+1167C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106697613 | |||||||
| chr12:106697717 | A | C | 1 | a0001c0002t0001g0136 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.833+1271A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106697717 | |||||||
| chr12:106697817 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.833+1371G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106697817 | |||||||
| chr12:106697979 | A | T | 4 | a0001c0001t0001g0107 a0001c0002t0001g0002 a0001c0002t0001g0058 others(1): Show |
4 | HG01884.hp2 HG02027.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.833+1533A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106697979 | |||||||
| chr12:106697982 | T | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0083 |
2 | HG00609.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.833+1536T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106697982 | |||||||
| chr12:106698026 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.833+1580G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106698026 | |||||||
| chr12:106698034 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.833+1588G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106698034 | |||||||
| chr12:106698521 | G | A | 130 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.833+2075G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106698521 | |||||||
| chr12:106698592 | C | T | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.833+2146C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106698592 | |||||||
| chr12:106698647 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.833+2201T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106698647 | |||||||
| chr12:106698732 | T | G | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.833+2286T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106698732 | |||||||
| chr12:106698757 | A | ATCT | 7 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.833+2311_833+2312i others(5): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106698757 | |||||||
| chr12:106698965 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02257.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.833+2519C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106698965 | |||||||
| chr12:106698977 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.833+2531T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106698977 | |||||||
| chr12:106699038 | G | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.833+2592G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106699038 | |||||||
| chr12:106699301 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.833+2855G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106699301 | |||||||
| chr12:106699341 | T | C | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.833+2895T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106699341 | |||||||
| chr12:106699375 | G | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.833+2929G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106699375 | |||||||
| chr12:106699428 | A | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0060 others(4): Show |
7 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.833+2982A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106699428 | |||||||
| chr12:106699572 | G | C | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.833+3126G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106699572 | |||||||
| chr12:106699675 | T | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.833+3229T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106699675 | |||||||
| chr12:106699730 | C | T | 3 | a0001c0002t0001g0042 a0001c0002t0001g0044 a0001c0002t0001g0046 |
3 | HG01081.hp1 HG01106.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.833+3284C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106699730 | |||||||
| chr12:106699807 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.833+3361G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106699807 | |||||||
| chr12:106700296 | C | T | 1 | a0001c0002t0001g0051 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.833+3850C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106700296 | |||||||
| chr12:106700324 | G | A | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.833+3878G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106700324 | |||||||
| chr12:106700381 | TAAGTTTG others(317): Show |
T | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.833+3952_833+4275d others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106700381 | ||||||
| chr12:106700403 | C | CT | 13 | a0001c0001t0001g0084 a0001c0001t0001g0092 a0001c0001t0001g0111 others(10): Show |
13 | HG01069.hp1 HG02027.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.833+3978dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106700403 | ||||||
| chr12:106700403 | CT | C | 20 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(17): Show |
20 | HG00609.hp1 HG01099.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.833+3978delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106700403 | ||||||
| chr12:106700403 | CTT | C | 8 | a0001c0002t0001g0034 a0001c0002t0001g0038 a0001c0002t0001g0039 others(5): Show |
8 | HG00408.hp2 HG02056.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+3977_833+3978d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106700403 | ||||||
| chr12:106700409 | T | C | 21 | a0001c0001t0001g0088 a0001c0001t0001g0194 a0001c0001t0001g0209 others(18): Show |
21 | HG00741.hp2 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.833+3963T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106700409 | |||||||
| chr12:106700499 | C | T | 3 | a0001c0002t0001g0137 a0001c0002t0001g0138 a0001c0002t0001g0139 |
3 | HG01099.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.833+4053C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106700499 | |||||||
| chr12:106700555 | A | C | 131 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(128): Show |
131 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.833+4109A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106700555 | |||||||
| chr12:106700556 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.833+4110G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106700556 | |||||||
| chr12:106700642 | G | A | 1 | a0001c0002t0001g0053 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.833+4196G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106700642 | |||||||
| chr12:106700917 | T | C | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.833+4471T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106700917 | |||||||
| chr12:106701254 | G | A | 49 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.833+4808G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106701254 | |||||||
| chr12:106701301 | T | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.833+4855T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106701301 | |||||||
| chr12:106701378 | T | C | 1 | a0001c0002t0001g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.833+4932T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106701378 | |||||||
| chr12:106701449 | ATCT | A | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
85 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(82): Show |
intron_variant | MODIFIER | c.833+5010_833+5012d others(5): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106701449 | ||||||
| chr12:106701488 | A | G | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.833+5042A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106701488 | |||||||
| chr12:106701591 | A | G | 1 | a0001c0002t0001g0038 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.833+5145A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106701591 | |||||||
| chr12:106701762 | C | T | 4 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.833+5316C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106701762 | |||||||
| chr12:106701808 | G | C | 2 | a0001c0002t0001g0138 a0001c0002t0001g0139 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.833+5362G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106701808 | |||||||
| chr12:106701853 | C | T | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.833+5407C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106701853 | |||||||
| chr12:106701976 | C | T | 3 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0003c0006t0001g0116 |
3 | HG02630.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.833+5530C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106701976 | |||||||
| chr12:106702126 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833+5680T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106702126 | |||||||
| chr12:106702189 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0249 |
2 | NA18966.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.833+5743T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106702189 | |||||||
| chr12:106702275 | A | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.833+5829A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106702275 | |||||||
| chr12:106702357 | C | T | 6 | a0001c0003t0001g0009 a0001c0003t0001g0060 a0001c0003t0001g0109 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.833+5911C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106702357 | |||||||
| chr12:106702370 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG02572.hp2 HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.833+5924C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106702370 | |||||||
| chr12:106702485 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.833+6039A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106702485 | |||||||
| chr12:106702504 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.833+6058A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106702504 | |||||||
| chr12:106702654 | T | G | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.833+6208T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106702654 | |||||||
| chr12:106703108 | C | T | 3 | a0001c0002t0001g0127 a0001c0002t0001g0130 a0001c0002t0001g0133 |
3 | HG02145.hp1 HG04184.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.834-6222C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106703108 | |||||||
| chr12:106703194 | G | T | 2 | a0001c0003t0001g0141 a0001c0003t0001g0143 |
2 | HG01109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.834-6136G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106703194 | |||||||
| chr12:106703203 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.834-6127T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106703203 | |||||||
| chr12:106703417 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.834-5913T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106703417 | |||||||
| chr12:106703832 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.834-5498G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106703832 | |||||||
| chr12:106703886 | C | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.834-5444C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106703886 | |||||||
| chr12:106704058 | A | C | 112 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.834-5272A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704058 | |||||||
| chr12:106704065 | C | CA | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
76 | HG00621.hp2 HG00735.hp2 HG01074.hp2 others(73): Show |
intron_variant | MODIFIER | c.834-5239dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106704065 | ||||||
| chr12:106704065 | C | CAA | 33 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0055 others(30): Show |
33 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.834-5240_834-5239d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106704065 | ||||||
| chr12:106704065 | CA | C | 46 | a0001c0001t0001g0161 a0001c0001t0001g0213 a0001c0002t0001g0002 others(43): Show |
46 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.834-5239delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106704065 | ||||||
| chr12:106704065 | CAA | C | 11 | a0001c0002t0001g0068 a0001c0002t0006g0147 a0001c0003t0001g0009 others(8): Show |
11 | HG01109.hp2 HG02257.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.834-5240_834-5239d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106704065 | ||||||
| chr12:106704154 | A | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.834-5176A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704154 | |||||||
| chr12:106704257 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.834-5073G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704257 | |||||||
| chr12:106704317 | T | C | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.834-5013T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704317 | |||||||
| chr12:106704320 | C | T | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.834-5010C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704320 | |||||||
| chr12:106704441 | T | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.834-4889T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704441 | |||||||
| chr12:106704800 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.834-4530A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704800 | |||||||
| chr12:106704843 | G | A | 2 | a0001c0001t0001g0236 a0001c0004t0001g0101 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.834-4487G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704843 | |||||||
| chr12:106704853 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(1): Show |
4 | HG01243.hp2 HG02738.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.834-4477G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704853 | |||||||
| chr12:106704855 | C | T | 34 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(31): Show |
34 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.834-4475C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106704855 | |||||||
| chr12:106705279 | T | C | 112 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.834-4051T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705279 | |||||||
| chr12:106705304 | G | A | 1 | a0004c0008t0001g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.834-4026G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705304 | |||||||
| chr12:106705357 | C | T | 1 | a0001c0002t0001g0045 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.834-3973C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705357 | |||||||
| chr12:106705374 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.834-3956G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705374 | |||||||
| chr12:106705460 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.834-3870A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705460 | |||||||
| chr12:106705536 | A | G | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.834-3794A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705536 | |||||||
| chr12:106705765 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0083 |
2 | HG00609.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.834-3565C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705765 | |||||||
| chr12:106705782 | G | A | 1 | a0004c0008t0001g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.834-3548G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705782 | |||||||
| chr12:106705877 | C | T | 2 | a0001c0002t0001g0058 a0001c0002t0001g0068 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.834-3453C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705877 | |||||||
| chr12:106705973 | T | C | 1 | a0001c0002t0001g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.834-3357T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106705973 | |||||||
| chr12:106706044 | G | C | 4 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.834-3286G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706044 | |||||||
| chr12:106706105 | A | G | 115 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.834-3225A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706105 | |||||||
| chr12:106706120 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0004g0036 others(1): Show |
4 | HG01243.hp2 HG02738.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.834-3210T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706120 | |||||||
| chr12:106706175 | G | C | 1 | a0001c0001t0001g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.834-3155G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706175 | |||||||
| chr12:106706373 | T | C | 1 | a0001c0002t0001g0274 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.834-2957T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706373 | |||||||
| chr12:106706386 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.834-2944A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706386 | |||||||
| chr12:106706443 | G | A | 1 | a0001c0002t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.834-2887G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706443 | |||||||
| chr12:106706596 | A | G | 1 | a0001c0002t0001g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.834-2734A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706596 | |||||||
| chr12:106706622 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834-2708G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706622 | |||||||
| chr12:106706728 | G | A | 5 | a0001c0002t0001g0136 a0001c0002t0001g0140 a0001c0002t0001g0186 others(2): Show |
5 | HG01123.hp1 HG01516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.834-2602G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706728 | |||||||
| chr12:106706864 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.834-2466G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706864 | |||||||
| chr12:106706939 | T | C | 220 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(217): Show |
220 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.834-2391T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706939 | |||||||
| chr12:106706942 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.834-2388T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706942 | |||||||
| chr12:106706948 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.834-2382C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106706948 | |||||||
| chr12:106707134 | G | A | 49 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.834-2196G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106707134 | |||||||
| chr12:106707232 | A | G | 1 | a0001c0003t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.834-2098A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106707232 | |||||||
| chr12:106707301 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.834-2029G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106707301 | |||||||
| chr12:106707551 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.834-1779G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106707551 | |||||||
| chr12:106707662 | G | A | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.834-1668G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106707662 | |||||||
| chr12:106707785 | T | TTTG | 4 | a0001c0002t0001g0058 a0001c0002t0001g0068 a0001c0002t0001g0070 others(1): Show |
4 | HG02723.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.834-1524_834-1522d others(5): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106707785 | ||||||
| chr12:106707795 | T | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.834-1535T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106707795 | |||||||
| chr12:106707907 | T | C | 116 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.834-1423T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106707907 | |||||||
| chr12:106707908 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.834-1422G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106707908 | |||||||
| chr12:106707991 | G | A | 3 | a0001c0002t0001g0165 a0001c0002t0001g0180 a0001c0002t0001g0185 |
3 | HG01256.hp2 HG03704.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.834-1339G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106707991 | |||||||
| chr12:106708043 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0030 |
2 | NA18942.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.834-1287A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106708043 | |||||||
| chr12:106708066 | G | A | 2 | a0001c0002t0001g0176 a0001c0002t0001g0240 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.834-1264G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106708066 | |||||||
| chr12:106708325 | T | TTG | 3 | a0001c0002t0001g0002 a0001c0002t0001g0120 a0001c0002t0006g0147 |
3 | HG02027.hp1 HG03492.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.834-991_834-990dup others(2): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106708325 | ||||||
| chr12:106708343 | GT | G | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG02145.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.834-975delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 106708343 | ||||||
| chr12:106708430 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.834-900G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106708430 | |||||||
| chr12:106708496 | G | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.834-834G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106708496 | |||||||
| chr12:106708547 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.834-783G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106708547 | |||||||
| chr12:106708634 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.834-696G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106708634 | |||||||
| chr12:106709017 | G | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01361.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.834-313G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106709017 | |||||||
| chr12:106709072 | A | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.834-258A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 8/17 | chr12 | 106709072 | |||||||
| chr12:106709545 | C | A | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.934+115C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106709545 | |||||||
| chr12:106709648 | TAGAG | T | 54 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.934+221_934+224del others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 106709648 | ||||||
| chr12:106709687 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.934+257G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106709687 | |||||||
| chr12:106709764 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.934+334C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106709764 | |||||||
| chr12:106709767 | T | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
89 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.934+337T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106709767 | |||||||
| chr12:106709922 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.934+492G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106709922 | |||||||
| chr12:106710019 | C | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.934+589C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106710019 | |||||||
| chr12:106710108 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.934+678G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106710108 | |||||||
| chr12:106710169 | T | G | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.934+739T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106710169 | |||||||
| chr12:106710483 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.935-970T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106710483 | |||||||
| chr12:106710512 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.935-941T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106710512 | |||||||
| chr12:106710571 | A | G | 49 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.935-882A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106710571 | |||||||
| chr12:106710839 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.935-614A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106710839 | |||||||
| chr12:106711211 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.935-242C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106711211 | |||||||
| chr12:106711249 | C | T | 11 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0060 others(8): Show |
11 | HG01175.hp1 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.935-204C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106711249 | |||||||
| chr12:106711348 | C | T | 1 | a0001c0001t0001g0003 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.935-105C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 9/17 | chr12 | 106711348 | |||||||
| chr12:106711724 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.993+213C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106711724 | |||||||
| chr12:106711944 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.993+433G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106711944 | |||||||
| chr12:106712004 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.993+493G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106712004 | |||||||
| chr12:106712543 | G | C | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.993+1032G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106712543 | |||||||
| chr12:106712558 | G | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0234 |
2 | NA18942.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.993+1047G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106712558 | |||||||
| chr12:106712768 | G | A | 115 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.993+1257G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106712768 | |||||||
| chr12:106712773 | AT | A | 50 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.993+1263delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106712773 | |||||||
| chr12:106712815 | C | A | 11 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0060 others(8): Show |
11 | HG01175.hp1 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.993+1304C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106712815 | |||||||
| chr12:106712902 | C | T | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+1391C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106712902 | |||||||
| chr12:106713006 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.993+1495G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106713006 | |||||||
| chr12:106713015 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.993+1504C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106713015 | |||||||
| chr12:106713339 | C | A | 1 | a0001c0002t0001g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.993+1828C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106713339 | |||||||
| chr12:106713468 | T | TA | 5 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | HG02615.hp1 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-1929dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106713468 | ||||||
| chr12:106713556 | G | T | 107 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(104): Show |
107 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.994-1844G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106713556 | |||||||
| chr12:106713694 | T | C | 20 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(17): Show |
20 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.994-1706T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106713694 | |||||||
| chr12:106713831 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.994-1569A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106713831 | |||||||
| chr12:106714068 | C | CA | 42 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0149 others(39): Show |
42 | HG00438.hp1 HG00621.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.994-1309dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106714068 | ||||||
| chr12:106714068 | C | CAAAAAAA others(5): Show |
17 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0037 others(14): Show |
17 | HG00140.hp1 HG00408.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.994-1320_994-1309d others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106714068 | ||||||
| chr12:106714068 | C | CAAAAAAA others(6): Show |
21 | a0001c0002t0001g0015 a0001c0002t0001g0020 a0001c0002t0001g0021 others(18): Show |
21 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.994-1321_994-1309d others(15): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106714068 | ||||||
| chr12:106714068 | C | CAAAAAAA others(7): Show |
10 | a0001c0002t0001g0033 a0001c0002t0001g0043 a0001c0002t0001g0048 others(7): Show |
10 | HG00735.hp2 HG01952.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.994-1322_994-1309d others(16): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106714068 | ||||||
| chr12:106714068 | C | CAAAAAAA others(8): Show |
14 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0029 others(11): Show |
14 | HG01175.hp1 HG01243.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.994-1323_994-1309d others(17): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106714068 | ||||||
| chr12:106714068 | C | CAAAAAAA others(9): Show |
6 | a0001c0003t0001g0060 a0001c0003t0001g0109 a0001c0003t0001g0110 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.994-1324_994-1309d others(18): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106714068 | ||||||
| chr12:106714068 | C | CAAAAAAA others(10): Show |
2 | a0001c0002t0005g0061 a0001c0003t0001g0009 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.994-1325_994-1309d others(19): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106714068 | ||||||
| chr12:106714068 | C | CAAAAAAA others(11): Show |
1 | a0001c0003t0001g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.994-1326_994-1309d others(20): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106714068 | ||||||
| chr12:106714068 | CA | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0082 others(7): Show |
10 | HG01168.hp1 HG01517.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.994-1309delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 106714068 | ||||||
| chr12:106714092 | G | A | 2 | a0001c0002t0001g0176 a0001c0002t0001g0240 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.994-1308G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714092 | |||||||
| chr12:106714092 | G | T | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.994-1308G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714092 | |||||||
| chr12:106714094 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.994-1306A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714094 | |||||||
| chr12:106714128 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.994-1272T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714128 | |||||||
| chr12:106714168 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.994-1232C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714168 | |||||||
| chr12:106714359 | A | G | 48 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(45): Show |
48 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.994-1041A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714359 | |||||||
| chr12:106714373 | T | G | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.994-1027T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714373 | |||||||
| chr12:106714438 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.994-962A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714438 | |||||||
| chr12:106714537 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.994-863G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714537 | |||||||
| chr12:106714593 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.994-807G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714593 | |||||||
| chr12:106714594 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.994-806G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714594 | |||||||
| chr12:106714600 | A | G | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.994-800A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106714600 | |||||||
| chr12:106715058 | C | G | 57 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(54): Show |
57 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.994-342C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106715058 | |||||||
| chr12:106715230 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.994-170G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 10/17 | chr12 | 106715230 | |||||||
| chr12:106715618 | G | A | 1 | a0001c0003t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1138+74G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106715618 | |||||||
| chr12:106715755 | T | C | 1 | a0001c0002t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1138+211T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106715755 | |||||||
| chr12:106715759 | C | G | 1 | a0001c0004t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1138+215C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106715759 | |||||||
| chr12:106715843 | T | C | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1138+299T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106715843 | |||||||
| chr12:106715874 | C | T | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1138+330C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106715874 | |||||||
| chr12:106715973 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1138+429C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106715973 | |||||||
| chr12:106716007 | T | C | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1138+463T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106716007 | |||||||
| chr12:106716028 | A | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1138+484A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106716028 | |||||||
| chr12:106716110 | G | T | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1138+566G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106716110 | |||||||
| chr12:106716193 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0259 |
2 | NA18954.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1138+649C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106716193 | |||||||
| chr12:106716297 | G | A | 53 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1138+753G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106716297 | |||||||
| chr12:106716329 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1138+785G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106716329 | |||||||
| chr12:106716383 | C | T | 1 | a0001c0002t0001g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1138+839C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106716383 | |||||||
| chr12:106716578 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1138+1034C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106716578 | |||||||
| chr12:106717000 | C | CA | 60 | a0001c0001t0001g0079 a0001c0001t0001g0117 a0001c0001t0001g0149 others(57): Show |
60 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1138+1478dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 106717000 | ||||||
| chr12:106717000 | C | CAA | 12 | a0001c0001t0001g0227 a0001c0002t0001g0070 a0001c0002t0001g0071 others(9): Show |
12 | HG01175.hp2 HG01516.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.1138+1477_1138+147 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 106717000 | ||||||
| chr12:106717000 | CA | C | 7 | a0001c0001t0001g0166 a0001c0001t0001g0236 a0001c0001t0001g0286 others(4): Show |
7 | HG00639.hp1 HG01099.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1138+1478delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 106717000 | ||||||
| chr12:106717032 | G | A | 16 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0060 others(13): Show |
16 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1138+1488G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106717032 | |||||||
| chr12:106717344 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1138+1800C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106717344 | |||||||
| chr12:106717782 | A | G | 224 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(221): Show |
224 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1139-2178A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106717782 | |||||||
| chr12:106717820 | G | A | 3 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1139-2140G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106717820 | |||||||
| chr12:106718155 | ATGCCCAA others(82): Show |
A | 1 | a0001c0002t0001g0237 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1139-1804_1139-171 others(93): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718155 | |||||||
| chr12:106718162 | A | AGAGACCT others(5): Show |
1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1139-1798_1139-179 others(16): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718162 | |||||||
| chr12:106718165 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1139-1795G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718165 | |||||||
| chr12:106718175 | C | T | 52 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(49): Show |
52 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1139-1785C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718175 | |||||||
| chr12:106718259 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1139-1701G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718259 | |||||||
| chr12:106718346 | A | G | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1139-1614A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718346 | |||||||
| chr12:106718380 | A | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1139-1580A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718380 | |||||||
| chr12:106718550 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1139-1410A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718550 | |||||||
| chr12:106718746 | A | T | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1139-1214A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718746 | |||||||
| chr12:106718836 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1139-1124C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718836 | |||||||
| chr12:106718844 | T | C | 2 | a0001c0001t0001g0262 a0001c0002t0001g0018 |
2 | HG01433.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1139-1116T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718844 | |||||||
| chr12:106718845 | G | T | 2 | a0001c0001t0001g0262 a0001c0002t0001g0018 |
2 | HG01433.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1139-1115G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718845 | |||||||
| chr12:106718881 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1139-1079C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718881 | |||||||
| chr12:106718954 | C | CA | 50 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0170 others(47): Show |
50 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1139-988dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 106718954 | ||||||
| chr12:106718954 | CA | C | 52 | a0001c0001t0001g0092 a0001c0002t0001g0017 a0001c0002t0001g0018 others(49): Show |
52 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.1139-988delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 106718954 | ||||||
| chr12:106718979 | G | A | 1 | a0005c0007t0001g0081 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1139-981G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718979 | |||||||
| chr12:106718990 | C | T | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1139-970C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106718990 | |||||||
| chr12:106719016 | G | A | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1139-944G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106719016 | |||||||
| chr12:106719084 | T | C | 7 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1139-876T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106719084 | |||||||
| chr12:106719246 | G | T | 222 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
222 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1139-714G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106719246 | |||||||
| chr12:106719520 | T | C | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1139-440T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106719520 | |||||||
| chr12:106719537 | T | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1139-423T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106719537 | |||||||
| chr12:106719592 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1139-368C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106719592 | |||||||
| chr12:106719770 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1139-190A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106719770 | |||||||
| chr12:106719811 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1139-149T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 11/17 | chr12 | 106719811 | |||||||
| chr12:106720138 | A | G | 1 | a0001c0002t0001g0234 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1233+84A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 12/17 | chr12 | 106720138 | |||||||
| chr12:106720308 | C | A | 1 | a0001c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1233+254C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 12/17 | chr12 | 106720308 | |||||||
| chr12:106720364 | T | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1233+310T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 12/17 | chr12 | 106720364 | |||||||
| chr12:106720445 | G | A | 54 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(51): Show |
54 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1234-314G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 12/17 | chr12 | 106720445 | |||||||
| chr12:106720528 | G | T | 4 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-231G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 12/17 | chr12 | 106720528 | |||||||
| chr12:106720649 | A | G | 57 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(54): Show |
57 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1234-110A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 12/17 | chr12 | 106720649 | |||||||
| chr12:106720701 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1234-58G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 12/17 | chr12 | 106720701 | |||||||
| chr12:106721057 | G | A | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1351+181G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721057 | |||||||
| chr12:106721095 | A | C | 1 | a0001c0002t0001g0064 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1351+219A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721095 | |||||||
| chr12:106721098 | T | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0006g0147 |
3 | HG02027.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1351+222T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721098 | |||||||
| chr12:106721109 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1351+233G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721109 | |||||||
| chr12:106721154 | A | G | 57 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(54): Show |
57 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1351+278A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721154 | |||||||
| chr12:106721351 | C | T | 34 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(31): Show |
34 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.1351+475C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721351 | |||||||
| chr12:106721385 | C | G | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1351+509C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721385 | |||||||
| chr12:106721538 | A | C | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1351+662A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721538 | |||||||
| chr12:106721585 | T | C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1351+709T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721585 | |||||||
| chr12:106721734 | C | T | 4 | a0001c0002t0001g0136 a0001c0002t0001g0186 a0001c0002t0001g0188 others(1): Show |
4 | HG01123.hp1 HG01516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351+858C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721734 | |||||||
| chr12:106721787 | T | G | 1 | a0001c0002t0001g0045 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1351+911T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721787 | |||||||
| chr12:106721795 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1351+919A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106721795 | |||||||
| chr12:106722289 | T | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1351+1413T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106722289 | |||||||
| chr12:106722327 | C | A | 1 | a0001c0002t0001g0201 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1351+1451C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106722327 | |||||||
| chr12:106722344 | G | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1351+1468G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106722344 | |||||||
| chr12:106722813 | G | T | 1 | a0001c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1351+1937G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106722813 | |||||||
| chr12:106722885 | G | A | 1 | a0001c0003t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1351+2009G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106722885 | |||||||
| chr12:106723279 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1351+2403C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106723279 | |||||||
| chr12:106723503 | A | G | 54 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(51): Show |
54 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1351+2627A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106723503 | |||||||
| chr12:106723699 | A | G | 1 | a0001c0002t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1351+2823A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106723699 | |||||||
| chr12:106723743 | A | G | 116 | a0001c0001t0001g0242 a0001c0002t0001g0002 a0001c0002t0001g0013 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1351+2867A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106723743 | |||||||
| chr12:106723837 | G | A | 1 | a0001c0003t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1351+2961G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106723837 | |||||||
| chr12:106723911 | G | A | 1 | a0001c0002t0001g0252 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1351+3035G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106723911 | |||||||
| chr12:106724195 | T | C | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351+3319T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106724195 | |||||||
| chr12:106724211 | G | A | 1 | a0001c0002t0001g0237 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1351+3335G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106724211 | |||||||
| chr12:106724357 | C | T | 34 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(31): Show |
34 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.1351+3481C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106724357 | |||||||
| chr12:106724871 | G | C | 1 | a0001c0002t0001g0039 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1351+3995G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106724871 | |||||||
| chr12:106725012 | C | CA | 15 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0001g0199 others(12): Show |
15 | HG00609.hp1 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1351+4151dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 106725012 | ||||||
| chr12:106725186 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1351+4310G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106725186 | |||||||
| chr12:106725204 | T | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1351+4328T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106725204 | |||||||
| chr12:106725317 | A | AATTGTTA others(22): Show |
1 | a0001c0002t0001g0237 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1351+4442_1351+447 others(33): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 106725317 | ||||||
| chr12:106725331 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1351+4455G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106725331 | |||||||
| chr12:106725382 | A | G | 1 | a0001c0002t0001g0229 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1351+4506A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106725382 | |||||||
| chr12:106725539 | CTT | C | 11 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0060 others(8): Show |
11 | HG01175.hp1 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1351+4665_1351+466 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 106725539 | ||||||
| chr12:106725702 | G | A | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1351+4826G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106725702 | |||||||
| chr12:106725711 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1351+4835C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106725711 | |||||||
| chr12:106725922 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1351+5046T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106725922 | |||||||
| chr12:106726017 | C | T | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351+5141C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106726017 | |||||||
| chr12:106726172 | C | T | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1351+5296C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106726172 | |||||||
| chr12:106726202 | C | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1351+5326C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106726202 | |||||||
| chr12:106726246 | T | TA | 12 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0076 others(9): Show |
12 | HG01243.hp2 HG02056.hp1 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.1351+5384dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 106726246 | ||||||
| chr12:106726246 | TA | T | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1351+5384delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 106726246 | ||||||
| chr12:106726322 | A | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0212 |
2 | HG00140.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1351+5446A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106726322 | |||||||
| chr12:106726412 | C | T | 4 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351+5536C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106726412 | |||||||
| chr12:106726413 | C | T | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1351+5537C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106726413 | |||||||
| chr12:106726646 | C | T | 122 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(119): Show |
122 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1352-5484C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106726646 | |||||||
| chr12:106726809 | T | C | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1352-5321T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106726809 | |||||||
| chr12:106726858 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1352-5272G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106726858 | |||||||
| chr12:106727108 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352-5022A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106727108 | |||||||
| chr12:106727212 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352-4918A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106727212 | |||||||
| chr12:106727514 | G | C | 3 | a0001c0002t0001g0162 a0001c0002t0001g0163 a0001c0002t0001g0258 |
3 | NA18954.hp1 NA19010.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1352-4616G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106727514 | |||||||
| chr12:106727626 | G | GT | 59 | a0001c0001t0001g0251 a0001c0002t0001g0031 a0001c0002t0001g0059 others(56): Show |
59 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1352-4493dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 106727626 | ||||||
| chr12:106727682 | C | T | 3 | a0001c0001t0001g0105 a0001c0002t0001g0070 a0001c0002t0001g0071 |
3 | HG02723.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1352-4448C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106727682 | |||||||
| chr12:106727840 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1352-4290C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106727840 | |||||||
| chr12:106727870 | C | T | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1352-4260C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106727870 | |||||||
| chr12:106727908 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1352-4222C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106727908 | |||||||
| chr12:106727909 | G | A | 6 | a0001c0002t0001g0128 a0001c0002t0001g0129 a0001c0002t0001g0135 others(3): Show |
6 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-4221G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106727909 | |||||||
| chr12:106728108 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1352-4022T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728108 | |||||||
| chr12:106728174 | A | G | 111 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1352-3956A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728174 | |||||||
| chr12:106728236 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0249 |
2 | NA18966.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1352-3894C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728236 | |||||||
| chr12:106728297 | T | TCCTCATG others(309): Show |
8 | a0001c0003t0001g0009 a0001c0003t0001g0019 a0001c0003t0001g0072 others(5): Show |
8 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1352-3822_1352-382 others(320): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 106728297 | ||||||
| chr12:106728297 | T | TCCTCATG others(310): Show |
38 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(35): Show |
38 | HG00621.hp1 HG00639.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1352-3822_1352-382 others(321): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 106728297 | ||||||
| chr12:106728297 | T | TCCTCATG others(311): Show |
11 | a0001c0002t0001g0155 a0001c0002t0001g0163 a0001c0002t0001g0176 others(8): Show |
11 | HG00438.hp1 HG01175.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1352-3822_1352-382 others(322): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 106728297 | ||||||
| chr12:106728324 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1352-3806C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728324 | |||||||
| chr12:106728366 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0208 |
2 | HG02027.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1352-3764C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728366 | |||||||
| chr12:106728368 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1352-3762C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728368 | |||||||
| chr12:106728369 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1352-3761G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728369 | |||||||
| chr12:106728580 | G | A | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1352-3550G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728580 | |||||||
| chr12:106728622 | G | A | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1352-3508G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728622 | |||||||
| chr12:106728801 | A | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1352-3329A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728801 | |||||||
| chr12:106728840 | C | G | 1 | a0001c0001t0001g0291 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1352-3290C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728840 | |||||||
| chr12:106728936 | T | C | 4 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1352-3194T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106728936 | |||||||
| chr12:106729118 | A | G | 113 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1352-3012A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106729118 | |||||||
| chr12:106729411 | T | C | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1352-2719T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106729411 | |||||||
| chr12:106729488 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1352-2642G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106729488 | |||||||
| chr12:106729805 | T | C | 1 | a0001c0002t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1352-2325T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106729805 | |||||||
| chr12:106730210 | G | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1352-1920G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106730210 | |||||||
| chr12:106730253 | C | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352-1877C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106730253 | |||||||
| chr12:106730430 | T | C | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1352-1700T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106730430 | |||||||
| chr12:106730659 | C | T | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1352-1471C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106730659 | |||||||
| chr12:106730698 | A | G | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1352-1432A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106730698 | |||||||
| chr12:106730703 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1352-1427C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106730703 | |||||||
| chr12:106730726 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0264 a0001c0002t0001g0013 others(2): Show |
5 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1352-1404C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106730726 | |||||||
| chr12:106730926 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1352-1204G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106730926 | |||||||
| chr12:106730956 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1352-1174C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106730956 | |||||||
| chr12:106731082 | A | G | 1 | a0001c0002t0001g0051 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1352-1048A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106731082 | |||||||
| chr12:106731158 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1352-972G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106731158 | |||||||
| chr12:106731215 | G | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1352-915G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 13/17 | chr12 | 106731215 | |||||||
| chr12:106732287 | A | G | 50 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1471+38A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/17 | chr12 | 106732287 | |||||||
| chr12:106732333 | T | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0208 |
2 | HG02027.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1471+84T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/17 | chr12 | 106732333 | |||||||
| chr12:106732342 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1471+93A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/17 | chr12 | 106732342 | |||||||
| chr12:106732353 | T | C | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1471+104T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/17 | chr12 | 106732353 | |||||||
| chr12:106732388 | T | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1471+139T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/17 | chr12 | 106732388 | |||||||
| chr12:106732489 | C | G | 3 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 |
3 | HG02280.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1471+240C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/17 | chr12 | 106732489 | |||||||
| chr12:106732607 | C | T | 1 | a0001c0002t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1472-317C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/17 | chr12 | 106732607 | |||||||
| chr12:106732655 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0166 a0001c0001t0001g0193 |
3 | HG00738.hp1 HG01099.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1472-269G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/17 | chr12 | 106732655 | |||||||
| chr12:106732707 | G | GTAAA | 3 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0006g0147 |
3 | HG02027.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1472-196_1472-193d others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 106732707 | ||||||
| chr12:106733148 | C | T | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1633+63C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106733148 | |||||||
| chr12:106733297 | T | C | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1633+212T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106733297 | |||||||
| chr12:106733740 | G | A | 3 | a0001c0001t0001g0102 a0001c0002t0001g0174 a0001c0002t0001g0229 |
3 | NA18992.hp1 NA19002.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1633+655G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106733740 | |||||||
| chr12:106733926 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1633+841C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106733926 | |||||||
| chr12:106733927 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1633+842G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106733927 | |||||||
| chr12:106733953 | A | C | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1633+868A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106733953 | |||||||
| chr12:106734075 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1633+990A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734075 | |||||||
| chr12:106734174 | G | A | 49 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1633+1089G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734174 | |||||||
| chr12:106734312 | T | A | 224 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(221): Show |
224 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1633+1227T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734312 | |||||||
| chr12:106734413 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1633+1328T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734413 | |||||||
| chr12:106734453 | G | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1633+1368G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734453 | |||||||
| chr12:106734595 | C | CA | 112 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1633+1523dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106734595 | ||||||
| chr12:106734605 | A | C | 1 | a0001c0001t0001g0008 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1633+1520A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734605 | |||||||
| chr12:106734893 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1633+1808C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734893 | |||||||
| chr12:106734916 | G | C | 40 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(37): Show |
40 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1633+1831G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734916 | |||||||
| chr12:106734943 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1633+1858G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734943 | |||||||
| chr12:106734987 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1633+1902G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106734987 | |||||||
| chr12:106735019 | A | C | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1633+1934A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735019 | |||||||
| chr12:106735042 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1633+1957T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735042 | |||||||
| chr12:106735044 | T | TA | 16 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(13): Show |
16 | HG01168.hp1 HG01169.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1633+1975dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106735044 | ||||||
| chr12:106735044 | TA | T | 8 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0198 others(5): Show |
8 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1633+1975delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106735044 | ||||||
| chr12:106735151 | TAATAATT others(15): Show |
T | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1633+2071_1633+209 others(26): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106735151 | ||||||
| chr12:106735177 | A | T | 1 | a0001c0002t0001g0129 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1633+2092A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735177 | |||||||
| chr12:106735186 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1633+2101T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735186 | |||||||
| chr12:106735330 | G | A | 133 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(130): Show |
133 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1633+2245G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735330 | |||||||
| chr12:106735391 | G | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1633+2306G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735391 | |||||||
| chr12:106735492 | A | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG02572.hp2 HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1633+2407A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735492 | |||||||
| chr12:106735573 | A | C | 3 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0003c0006t0001g0116 |
3 | HG02630.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1633+2488A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735573 | |||||||
| chr12:106735619 | A | G | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1633+2534A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735619 | |||||||
| chr12:106735641 | G | A | 111 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1633+2556G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735641 | |||||||
| chr12:106735696 | AT | A | 124 | a0001c0001t0001g0111 a0001c0001t0001g0220 a0001c0001t0001g0221 others(121): Show |
124 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1633+2620delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106735696 | ||||||
| chr12:106735696 | ATT | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1633+2619_1633+262 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106735696 | ||||||
| chr12:106735863 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1633+2778G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735863 | |||||||
| chr12:106735941 | C | A | 55 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1633+2856C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106735941 | |||||||
| chr12:106736044 | C | A | 2 | a0001c0001t0001g0100 a0001c0002t0001g0274 |
2 | NA18956.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1633+2959C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106736044 | |||||||
| chr12:106736301 | C | T | 4 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633+3216C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106736301 | |||||||
| chr12:106736412 | T | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
89 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.1633+3327T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106736412 | |||||||
| chr12:106736719 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1633+3634G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106736719 | |||||||
| chr12:106736914 | C | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0193 |
2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1633+3829C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106736914 | |||||||
| chr12:106737130 | A | G | 4 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633+4045A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106737130 | |||||||
| chr12:106737162 | G | GT | 6 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0112 others(3): Show |
6 | HG02027.hp2 HG03704.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1633+4117dupT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0244 a0001c0002t0001g0238 |
2 | HG01106.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1633+4108_1633+411 others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GT | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(36): Show |
39 | HG00099.hp1 HG00621.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1633+4117delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTT | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(56): Show |
60 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1633+4116_1633+411 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTT | G | 53 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0075 others(50): Show |
53 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1633+4115_1633+411 others(7): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTT | G | 21 | a0001c0001t0001g0085 a0001c0001t0001g0095 a0001c0001t0001g0097 others(18): Show |
21 | HG00408.hp1 HG00735.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1633+4114_1633+411 others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTT | G | 8 | a0001c0001t0001g0089 a0001c0001t0001g0148 a0001c0001t0001g0230 others(5): Show |
8 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1633+4113_1633+411 others(9): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(3): Show |
G | 1 | a0001c0002t0001g0195 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1633+4108_1633+411 others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(4): Show |
G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0255 a0001c0002t0001g0135 |
3 | HG01069.hp1 HG06807.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1633+4107_1633+411 others(15): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(6): Show |
G | 1 | a0001c0002t0001g0015 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1633+4105_1633+411 others(17): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(7): Show |
G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0058 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1633+4104_1633+411 others(18): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(8): Show |
G | 3 | a0001c0002t0001g0127 a0001c0002t0001g0130 a0001c0002t0005g0061 |
3 | HG02109.hp2 HG02145.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1633+4103_1633+411 others(19): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(9): Show |
G | 4 | a0001c0002t0001g0070 a0001c0002t0001g0071 a0001c0003t0001g0019 others(1): Show |
4 | HG02723.hp2 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633+4102_1633+411 others(20): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(10): Show |
G | 13 | a0001c0001t0001g0270 a0001c0001t0001g0291 a0001c0003t0001g0009 others(10): Show |
13 | HG01109.hp2 HG01943.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1633+4101_1633+411 others(21): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(11): Show |
G | 40 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(37): Show |
40 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1633+4100_1633+411 others(22): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(12): Show |
G | 7 | a0001c0001t0001g0149 a0001c0001t0001g0194 a0001c0001t0001g0245 others(4): Show |
7 | HG00741.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1633+4099_1633+411 others(23): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(13): Show |
G | 2 | a0001c0001t0001g0290 a0004c0008t0001g0146 |
2 | HG02717.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1633+4098_1633+411 others(24): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(15): Show |
G | 1 | a0001c0002t0001g0038 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1633+4096_1633+411 others(26): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737162 | GTTTTTTT others(17): Show |
G | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1633+4094_1633+411 others(28): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737162 | ||||||
| chr12:106737174 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1633+4089T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106737174 | |||||||
| chr12:106737179 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1633+4094T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106737179 | |||||||
| chr12:106737237 | C | T | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1633+4152C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106737237 | |||||||
| chr12:106737536 | A | G | 115 | a0001c0001t0001g0242 a0001c0002t0001g0002 a0001c0002t0001g0013 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1633+4451A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106737536 | |||||||
| chr12:106737642 | T | TAAGAAAC others(322): Show |
1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1633+4571_1633+457 others(333): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106737642 | ||||||
| chr12:106737812 | T | A | 1 | a0004c0008t0001g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1633+4727T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106737812 | |||||||
| chr12:106737864 | C | A | 1 | a0001c0002t0001g0229 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1633+4779C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106737864 | |||||||
| chr12:106737944 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1633+4859G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106737944 | |||||||
| chr12:106737984 | T | C | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1633+4899T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106737984 | |||||||
| chr12:106738508 | A | G | 1 | a0001c0002t0001g0042 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1633+5423A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106738508 | |||||||
| chr12:106738645 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1633+5560G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106738645 | |||||||
| chr12:106738723 | A | G | 111 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1633+5638A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106738723 | |||||||
| chr12:106738909 | GTA | G | 5 | a0001c0002t0001g0155 a0001c0002t0001g0174 a0001c0002t0001g0229 others(2): Show |
5 | HG02135.hp2 NA18747.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1633+5825_1633+582 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106738909 | |||||||
| chr12:106739030 | AT | A | 49 | a0001c0001t0001g0242 a0001c0002t0001g0017 a0001c0002t0001g0018 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1633+5946delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739030 | |||||||
| chr12:106739052 | T | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1633+5967T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739052 | |||||||
| chr12:106739104 | T | C | 4 | a0001c0002t0001g0127 a0001c0002t0001g0130 a0001c0002t0001g0133 others(1): Show |
4 | HG02145.hp1 HG03831.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633+6019T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739104 | |||||||
| chr12:106739108 | G | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1633+6023G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739108 | |||||||
| chr12:106739125 | C | CAGAA | 10 | a0001c0001t0001g0181 a0001c0002t0001g0037 a0001c0002t0001g0068 others(7): Show |
10 | HG01175.hp1 HG01943.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1633+6066_1633+606 others(8): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106739125 | ||||||
| chr12:106739125 | C | CAGAAAGA others(1): Show |
37 | a0001c0002t0001g0031 a0001c0002t0001g0056 a0001c0002t0001g0059 others(34): Show |
37 | HG00438.hp1 HG00621.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.1633+6062_1633+606 others(12): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106739125 | ||||||
| chr12:106739125 | C | CAGAAAGA others(5): Show |
4 | a0001c0002t0001g0057 a0001c0002t0001g0162 a0001c0002t0001g0163 others(1): Show |
4 | HG01175.hp2 HG04115.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633+6058_1633+606 others(16): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106739125 | ||||||
| chr12:106739125 | C | CAGAAAGA others(9): Show |
27 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(24): Show |
27 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1633+6054_1633+606 others(20): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106739125 | ||||||
| chr12:106739125 | C | CAGAAAGA others(13): Show |
23 | a0001c0001t0001g0242 a0001c0002t0001g0017 a0001c0002t0001g0018 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1633+6050_1633+606 others(24): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106739125 | ||||||
| chr12:106739125 | C | CAGAAAGA others(17): Show |
2 | a0001c0002t0001g0120 a0001c0002t0001g0137 |
2 | HG01099.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1633+6046_1633+606 others(28): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106739125 | ||||||
| chr12:106739300 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1633+6215T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739300 | |||||||
| chr12:106739350 | T | A | 2 | a0001c0003t0001g0060 a0001c0003t0001g0228 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1633+6265T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739350 | |||||||
| chr12:106739406 | T | C | 40 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(37): Show |
40 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1633+6321T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739406 | |||||||
| chr12:106739468 | C | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1633+6383C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739468 | |||||||
| chr12:106739623 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1633+6538G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739623 | |||||||
| chr12:106739700 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1633+6615C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739700 | |||||||
| chr12:106739973 | C | T | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+6888C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739973 | |||||||
| chr12:106739997 | C | T | 111 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1633+6912C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106739997 | |||||||
| chr12:106740245 | G | T | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1633+7160G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106740245 | |||||||
| chr12:106740409 | A | G | 4 | a0001c0002t0001g0059 a0001c0002t0001g0157 a0001c0002t0001g0179 others(1): Show |
4 | HG01167.hp1 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634-7028A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106740409 | |||||||
| chr12:106740518 | C | G | 1 | a0001c0002t0001g0258 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1634-6919C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106740518 | |||||||
| chr12:106740650 | A | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0086 others(14): Show |
17 | HG00408.hp1 HG00438.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1634-6787A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106740650 | |||||||
| chr12:106740788 | G | T | 55 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1634-6649G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106740788 | |||||||
| chr12:106740815 | G | GA | 141 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0085 others(138): Show |
141 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1634-6621dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106740815 | ||||||
| chr12:106741367 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1634-6070T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106741367 | |||||||
| chr12:106741517 | A | C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1634-5920A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106741517 | |||||||
| chr12:106741592 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1634-5845G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106741592 | |||||||
| chr12:106741771 | G | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0264 |
2 | NA18951.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1634-5666G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106741771 | |||||||
| chr12:106741807 | G | T | 1 | a0001c0003t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1634-5630G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106741807 | |||||||
| chr12:106741869 | G | A | 113 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1634-5568G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106741869 | |||||||
| chr12:106741894 | A | C | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1634-5543A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106741894 | |||||||
| chr12:106742062 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0166 a0001c0001t0001g0193 |
3 | HG00738.hp1 HG01099.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1634-5375G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106742062 | |||||||
| chr12:106742164 | A | G | 111 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1634-5273A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106742164 | |||||||
| chr12:106742213 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1634-5224G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106742213 | |||||||
| chr12:106742674 | A | C | 1 | a0001c0002t0001g0031 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1634-4763A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106742674 | |||||||
| chr12:106742918 | T | G | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-4519T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106742918 | |||||||
| chr12:106743090 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1634-4347A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743090 | |||||||
| chr12:106743246 | C | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1634-4191C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743246 | |||||||
| chr12:106743592 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1634-3845C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743592 | |||||||
| chr12:106743749 | G | A | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1634-3688G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743749 | |||||||
| chr12:106743757 | C | A | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1634-3680C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743757 | |||||||
| chr12:106743757 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1634-3680C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743757 | |||||||
| chr12:106743801 | C | A | 2 | a0001c0002t0001g0119 a0001c0002t0001g0121 |
2 | HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1634-3636C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743801 | |||||||
| chr12:106743822 | C | T | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1634-3615C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743822 | |||||||
| chr12:106743832 | G | A | 3 | a0001c0003t0001g0009 a0001c0003t0001g0060 a0001c0003t0001g0228 |
3 | HG02257.hp1 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1634-3605G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743832 | |||||||
| chr12:106743840 | T | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1634-3597T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106743840 | |||||||
| chr12:106744363 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | NA18982.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1634-3074C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106744363 | |||||||
| chr12:106744580 | A | G | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-2857A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106744580 | |||||||
| chr12:106744588 | G | T | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1634-2849G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106744588 | |||||||
| chr12:106744840 | T | G | 1 | a0001c0002t0001g0129 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1634-2597T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106744840 | |||||||
| chr12:106744843 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1634-2594T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106744843 | |||||||
| chr12:106744854 | T | G | 1 | a0001c0003t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1634-2583T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106744854 | |||||||
| chr12:106745360 | A | C | 1 | a0001c0001t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1634-2077A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106745360 | |||||||
| chr12:106745762 | A | G | 111 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1634-1675A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106745762 | |||||||
| chr12:106745907 | A | C | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634-1530A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106745907 | |||||||
| chr12:106745993 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1634-1444G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106745993 | |||||||
| chr12:106746095 | C | T | 1 | a0001c0002t0001g0234 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1634-1342C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106746095 | |||||||
| chr12:106746128 | C | T | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0155 others(2): Show |
5 | HG01516.hp1 HG01517.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1634-1309C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106746128 | |||||||
| chr12:106746205 | T | A | 115 | a0001c0001t0001g0242 a0001c0002t0001g0002 a0001c0002t0001g0013 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1634-1232T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106746205 | |||||||
| chr12:106746243 | C | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1634-1194C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106746243 | |||||||
| chr12:106746282 | G | C | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1634-1155G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106746282 | |||||||
| chr12:106746355 | C | CA | 36 | a0001c0001t0001g0080 a0001c0001t0001g0156 a0001c0001t0001g0158 others(33): Show |
36 | HG01071.hp1 HG01109.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1634-1062dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106746355 | ||||||
| chr12:106746355 | CA | C | 8 | a0001c0001t0001g0090 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG02074.hp1 HG02109.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1634-1062delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106746355 | ||||||
| chr12:106746461 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1634-976G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106746461 | |||||||
| chr12:106746507 | G | A | 5 | a0001c0002t0001g0238 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634-930G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106746507 | |||||||
| chr12:106746538 | CA | C | 7 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-889delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 106746538 | ||||||
| chr12:106746858 | C | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0103 others(1): Show |
4 | HG03041.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634-579C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106746858 | |||||||
| chr12:106746933 | T | C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01168.hp1 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1634-504T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106746933 | |||||||
| chr12:106747012 | A | G | 115 | a0001c0001t0001g0242 a0001c0002t0001g0002 a0001c0002t0001g0013 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1634-425A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106747012 | |||||||
| chr12:106747017 | G | A | 4 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-420G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106747017 | |||||||
| chr12:106747107 | T | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1634-330T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106747107 | |||||||
| chr12:106747191 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1634-246C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106747191 | |||||||
| chr12:106747296 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1634-141G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106747296 | |||||||
| chr12:106747334 | A | G | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1634-103A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 15/17 | chr12 | 106747334 | |||||||
| chr12:106747725 | C | T | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1796+126C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106747725 | |||||||
| chr12:106747898 | A | C | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1796+299A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106747898 | |||||||
| chr12:106747915 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1796+316G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106747915 | |||||||
| chr12:106747927 | T | TAA | 51 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(48): Show |
51 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1796+343_1796+344d others(4): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 106747927 | ||||||
| chr12:106747927 | TA | T | 14 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(11): Show |
14 | HG01517.hp2 HG01884.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1796+344delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 106747927 | ||||||
| chr12:106748022 | G | A | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1796+423G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748022 | |||||||
| chr12:106748170 | G | A | 37 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(34): Show |
37 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1796+571G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748170 | |||||||
| chr12:106748189 | A | G | 57 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(54): Show |
57 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1796+590A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748189 | |||||||
| chr12:106748235 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1796+636T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748235 | |||||||
| chr12:106748478 | T | C | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1796+879T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748478 | |||||||
| chr12:106748520 | T | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1796+921T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748520 | |||||||
| chr12:106748529 | T | A | 3 | a0001c0002t0001g0165 a0001c0002t0001g0180 a0001c0002t0001g0185 |
3 | HG01256.hp2 HG03704.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1796+930T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748529 | |||||||
| chr12:106748662 | A | G | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1796+1063A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748662 | |||||||
| chr12:106748857 | G | A | 57 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(54): Show |
57 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1796+1258G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748857 | |||||||
| chr12:106748903 | G | A | 50 | a0001c0001t0001g0242 a0001c0002t0001g0017 a0001c0002t0001g0018 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1796+1304G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748903 | |||||||
| chr12:106748946 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1796+1347G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106748946 | |||||||
| chr12:106749079 | A | C | 1 | a0001c0001t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1796+1480A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749079 | |||||||
| chr12:106749083 | C | CA | 21 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(18): Show |
21 | HG01074.hp2 HG01255.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1796+1499dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 106749083 | ||||||
| chr12:106749115 | T | G | 1 | a0001c0002t0001g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1796+1516T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749115 | |||||||
| chr12:106749192 | G | A | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1797-1463G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749192 | |||||||
| chr12:106749214 | C | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0203 |
2 | HG00735.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1797-1441C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749214 | |||||||
| chr12:106749242 | C | T | 1 | a0001c0002t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1797-1413C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749242 | |||||||
| chr12:106749257 | C | CA | 19 | a0001c0001t0001g0114 a0001c0001t0001g0190 a0001c0001t0001g0233 others(16): Show |
19 | HG01074.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1797-1378dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 106749257 | ||||||
| chr12:106749257 | CA | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0230 a0001c0002t0001g0056 others(4): Show |
7 | HG01168.hp1 HG01168.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1797-1378delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 106749257 | ||||||
| chr12:106749348 | G | C | 112 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1797-1307G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749348 | |||||||
| chr12:106749482 | T | C | 117 | a0001c0001t0001g0242 a0001c0002t0001g0002 a0001c0002t0001g0013 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1797-1173T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749482 | |||||||
| chr12:106749483 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1797-1172G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749483 | |||||||
| chr12:106749518 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1797-1137G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749518 | |||||||
| chr12:106749524 | T | C | 1 | a0001c0002t0005g0061 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1797-1131T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749524 | |||||||
| chr12:106749775 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1797-880G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749775 | |||||||
| chr12:106749802 | C | T | 6 | a0001c0002t0001g0063 a0001c0002t0001g0065 a0001c0002t0001g0066 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1797-853C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749802 | |||||||
| chr12:106749849 | G | A | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0263 others(4): Show |
7 | HG02027.hp1 NA18982.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.1797-806G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749849 | |||||||
| chr12:106749867 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1797-788C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749867 | |||||||
| chr12:106749894 | C | T | 1 | a0001c0003t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1797-761C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749894 | |||||||
| chr12:106749916 | G | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1797-739G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106749916 | |||||||
| chr12:106750073 | C | T | 7 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | NA18948.hp1 NA18964.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1797-582C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106750073 | |||||||
| chr12:106750090 | G | A | 4 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0103 others(1): Show |
4 | HG03041.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797-565G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106750090 | |||||||
| chr12:106750334 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1797-321G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106750334 | |||||||
| chr12:106750408 | C | T | 113 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1797-247C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106750408 | |||||||
| chr12:106750456 | A | G | 1 | a0001c0003t0001g0110 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1797-199A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106750456 | |||||||
| chr12:106750476 | C | CA | 14 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0224 others(11): Show |
14 | HG01123.hp2 HG01175.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1797-163dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 106750476 | ||||||
| chr12:106750476 | CA | C | 7 | a0001c0001t0001g0023 a0001c0002t0001g0013 a0001c0002t0001g0014 others(4): Show |
7 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1797-163delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr12 | 106750476 | ||||||
| chr12:106750484 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1797-171A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106750484 | |||||||
| chr12:106750506 | G | A | 2 | a0001c0002t0001g0058 a0001c0002t0001g0135 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1797-149G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106750506 | |||||||
| chr12:106750550 | A | G | 125 | a0001c0001t0001g0242 a0001c0002t0001g0002 a0001c0002t0001g0013 others(122): Show |
125 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1797-105A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106750550 | |||||||
| chr12:106750555 | G | A | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02145.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1797-100G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 16/17 | chr12 | 106750555 | |||||||
| chr12:106750894 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1935+101G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106750894 | |||||||
| chr12:106750920 | C | CTTTA | 49 | a0001c0001t0001g0242 a0001c0002t0001g0002 a0001c0002t0001g0031 others(46): Show |
49 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1935+147_1935+150d others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 106750920 | ||||||
| chr12:106750920 | C | CTTTATTT others(1): Show |
66 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1935+143_1935+150d others(10): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 106750920 | ||||||
| chr12:106750920 | C | CTTTATTT others(5): Show |
2 | a0001c0002t0001g0135 a0001c0002t0005g0061 |
2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1935+139_1935+150d others(14): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 106750920 | ||||||
| chr12:106751168 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1935+375T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106751168 | |||||||
| chr12:106751173 | G | T | 57 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(54): Show |
57 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1935+380G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106751173 | |||||||
| chr12:106751206 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1935+413G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106751206 | |||||||
| chr12:106751347 | T | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1935+554T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106751347 | |||||||
| chr12:106751381 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | NA18982.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1935+588A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106751381 | |||||||
| chr12:106751514 | T | C | 2 | a0001c0002t0001g0013 a0001c0002t0001g0014 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1935+721T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106751514 | |||||||
| chr12:106751787 | C | T | 2 | a0001c0002t0001g0058 a0001c0002t0001g0135 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1935+994C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106751787 | |||||||
| chr12:106751951 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1935+1158A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106751951 | |||||||
| chr12:106751996 | A | G | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1935+1203A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106751996 | |||||||
| chr12:106752009 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1935+1216G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752009 | |||||||
| chr12:106752053 | G | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0123 |
3 | HG03139.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1935+1260G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752053 | |||||||
| chr12:106752157 | G | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0154 a0001c0001t0001g0202 others(1): Show |
4 | HG02135.hp1 NA18943.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1935+1364G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752157 | |||||||
| chr12:106752255 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1935+1462C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752255 | |||||||
| chr12:106752280 | C | T | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1935+1487C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752280 | |||||||
| chr12:106752400 | G | A | 3 | a0001c0002t0001g0058 a0001c0002t0001g0135 a0001c0002t0005g0061 |
3 | HG02109.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1935+1607G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752400 | |||||||
| chr12:106752437 | G | T | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1935+1644G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752437 | |||||||
| chr12:106752439 | C | T | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1935+1646C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752439 | |||||||
| chr12:106752463 | C | A | 55 | a0001c0001t0001g0242 a0001c0002t0001g0013 a0001c0002t0001g0014 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1935+1670C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752463 | |||||||
| chr12:106752598 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0030 |
2 | NA18942.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1935+1805G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752598 | |||||||
| chr12:106752986 | A | C | 2 | a0001c0002t0001g0070 a0001c0002t0001g0071 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1935+2193A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106752986 | |||||||
| chr12:106753191 | A | G | 1 | a0001c0003t0001g0072 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1935+2398A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106753191 | |||||||
| chr12:106753303 | C | G | 57 | a0001c0002t0001g0031 a0001c0002t0001g0059 a0001c0002t0001g0136 others(54): Show |
57 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1935+2510C>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106753303 | |||||||
| chr12:106753392 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1935+2599C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106753392 | |||||||
| chr12:106753684 | T | C | 1 | a0001c0002t0001g0185 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1935+2891T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106753684 | |||||||
| chr12:106753764 | T | C | 49 | a0001c0001t0001g0242 a0001c0002t0001g0017 a0001c0002t0001g0018 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1935+2971T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106753764 | |||||||
| chr12:106753865 | G | A | 2 | a0001c0002t0001g0058 a0001c0002t0001g0135 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1935+3072G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106753865 | |||||||
| chr12:106753980 | A | T | 1 | a0001c0001t0001g0190 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1935+3187A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106753980 | |||||||
| chr12:106753992 | G | A | 2 | a0001c0002t0001g0058 a0001c0002t0001g0135 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1935+3199G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106753992 | |||||||
| chr12:106754143 | G | A | 6 | a0001c0002t0001g0063 a0001c0002t0001g0065 a0001c0002t0001g0066 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1935+3350G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106754143 | |||||||
| chr12:106754231 | G | A | 1 | a0001c0002t0001g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1935+3438G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106754231 | |||||||
| chr12:106754402 | A | T | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1935+3609A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106754402 | |||||||
| chr12:106754706 | T | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0249 |
2 | NA18966.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1935+3913T>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106754706 | |||||||
| chr12:106754799 | G | T | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1935+4006G>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106754799 | |||||||
| chr12:106754824 | C | A | 1 | a0001c0002t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1935+4031C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106754824 | |||||||
| chr12:106754824 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(71): Show |
74 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.1935+4031C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106754824 | |||||||
| chr12:106754838 | A | G | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1935+4045A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106754838 | |||||||
| chr12:106755024 | A | G | 2 | a0001c0002t0001g0058 a0001c0002t0001g0135 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1935+4231A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106755024 | |||||||
| chr12:106755105 | A | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
96 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(93): Show |
intron_variant | MODIFIER | c.1935+4312A>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106755105 | |||||||
| chr12:106755158 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1935+4365G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106755158 | |||||||
| chr12:106755234 | C | T | 91 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
91 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(88): Show |
intron_variant | MODIFIER | c.1935+4441C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106755234 | |||||||
| chr12:106755315 | C | T | 3 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 |
3 | HG02135.hp2 NA18951.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1935+4522C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106755315 | |||||||
| chr12:106755378 | G | A | 29 | a0001c0001t0001g0242 a0001c0002t0001g0021 a0001c0002t0001g0032 others(26): Show |
29 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1935+4585G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106755378 | |||||||
| chr12:106755558 | G | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+4765G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106755558 | |||||||
| chr12:106755644 | A | T | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
208 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1935+4851A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106755644 | |||||||
| chr12:106756288 | C | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1936-4909C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106756288 | |||||||
| chr12:106756373 | G | A | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1936-4824G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106756373 | |||||||
| chr12:106756383 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG01258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1936-4814C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106756383 | |||||||
| chr12:106756504 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1936-4693T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106756504 | |||||||
| chr12:106756527 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1936-4670G>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106756527 | |||||||
| chr12:106756564 | GA | G | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
150 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1936-4621delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 106756564 | ||||||
| chr12:106756931 | G | A | 11 | a0001c0002t0001g0021 a0001c0002t0001g0032 a0001c0002t0001g0041 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1936-4266G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106756931 | |||||||
| chr12:106757062 | C | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0285 |
2 | HG02602.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1936-4135C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106757062 | |||||||
| chr12:106757068 | T | C | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1936-4129T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106757068 | |||||||
| chr12:106757139 | A | C | 1 | a0001c0002t0001g0064 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1936-4058A>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106757139 | |||||||
| chr12:106757172 | T | G | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02145.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-4025T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106757172 | |||||||
| chr12:106757547 | C | CA | 16 | a0001c0001t0001g0108 a0001c0001t0001g0117 a0001c0001t0001g0156 others(13): Show |
16 | HG01099.hp1 HG01496.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.1936-3631dupA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 106757547 | ||||||
| chr12:106757547 | CA | C | 10 | a0001c0001t0001g0161 a0001c0001t0001g0242 a0001c0002t0001g0041 others(7): Show |
10 | HG00639.hp1 HG01169.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.1936-3631delA | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 106757547 | ||||||
| chr12:106757920 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1936-3277C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106757920 | |||||||
| chr12:106758185 | G | A | 1 | a0001c0002t0006g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1936-3012G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106758185 | |||||||
| chr12:106758319 | G | A | 1 | a0002c0005t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1936-2878G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106758319 | |||||||
| chr12:106758628 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1936-2569T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106758628 | |||||||
| chr12:106758916 | T | G | 2 | a0001c0002t0001g0176 a0001c0002t0001g0240 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1936-2281T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106758916 | |||||||
| chr12:106758974 | T | C | 2 | a0001c0002t0001g0002 a0001c0002t0006g0147 |
2 | HG02027.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1936-2223T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106758974 | |||||||
| chr12:106759022 | AT | A | 4 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0103 others(1): Show |
4 | HG03041.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1936-2174delT | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106759022 | |||||||
| chr12:106759025 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1936-2172G>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106759025 | |||||||
| chr12:106759336 | A | AGG | 38 | a0001c0001t0001g0161 a0001c0002t0001g0031 a0001c0002t0001g0059 others(35): Show |
38 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1936-1859_1936-185 others(6): Show |
RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 106759336 | ||||||
| chr12:106759383 | C | T | 4 | a0001c0003t0001g0141 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1936-1814C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106759383 | |||||||
| chr12:106759389 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1936-1808T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106759389 | |||||||
| chr12:106759594 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1936-1603C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106759594 | |||||||
| chr12:106759705 | C | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0123 |
3 | HG03139.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1936-1492C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106759705 | |||||||
| chr12:106759832 | T | C | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1936-1365T>C | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106759832 | |||||||
| chr12:106759995 | T | G | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1936-1202T>G | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106759995 | |||||||
| chr12:106760093 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0086 |
2 | HG00438.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1936-1104C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106760093 | |||||||
| chr12:106760272 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1936-925A>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106760272 | |||||||
| chr12:106760302 | C | A | 1 | a0001c0002t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1936-895C>A | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106760302 | |||||||
| chr12:106760841 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1936-356C>T | RFX4 | ENSG00000111783.13 | transcript | ENST00000392842.6 | protein_coding | 17/17 | chr12 | 106760841 |