Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84282 |
| ensemblid | ENSG00000181481.14 |
| hgncid | 21158 |
| symbol | RNF135 |
| name | ring finger protein 135 |
| refseq_nuc | NM_032322.4 |
| refseq_prot | NP_115698.3 |
| ensembl_nuc | ENST00000328381.10 |
| ensembl_prot | ENSP00000328340.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 30971039 |
| end | 30999911 |
| strand | + |
| ver | v1.2 |
| region | chr17:30971039-30999911 |
| region5000 | chr17:30966039-31004911 |
| regionname0 | RNF135_chr17_30971039_30999911 |
| regionname5000 | RNF135_chr17_30966039_31004911 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 432 | 182 | 14 | 58 | 70 | 12 | 26 | 42 | RNF135_chr17_30966039_31004911 | RNF135 | MAGLG others(427): Show |
chr17 | 30966039 | 31004911 |
| a0002 | 0/0 | 432 | 66 | 58 | 8 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | MAGLG others(427): Show |
chr17 | 30966039 | 31004911 |
| a0003 | 0/0 | 432 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | MAGLG others(427): Show |
chr17 | 30966039 | 31004911 |
| a0004 | 0/0 | 432 | 4 | 1 | 1 | 0 | 2 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | MAGLG others(427): Show |
chr17 | 30966039 | 31004911 |
| a0005 | 0/0 | 432 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | MAGLG others(427): Show |
chr17 | 30966039 | 31004911 |
| a0006 | 0/0 | 432 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | MAGLG others(427): Show |
chr17 | 30966039 | 31004911 |
| a0007 | 0/0 | 432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | MAGLG others(427): Show |
chr17 | 30966039 | 31004911 |
| a0008 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | MAGLG others(427): Show |
chr17 | 30966039 | 31004911 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1296 | 182 | 14 | 58 | 70 | 12 | 26 | RNF135_chr17_30966039_31004911 | RNF135 | ATGGC others(1291): Show |
chr17 | 30966039 | 31004911 | ||
| a0002c0002 | 0/0 | 1296 | 62 | 54 | 8 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | ATGGC others(1291): Show |
chr17 | 30966039 | 31004911 | ||
| a0002c0006 | 0/0 | 1296 | 4 | 4 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | ATGGC others(1291): Show |
chr17 | 30966039 | 31004911 | ||
| a0003c0003 | 0/0 | 1296 | 5 | 5 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | ATGGC others(1291): Show |
chr17 | 30966039 | 31004911 | ||
| a0004c0004 | 0/0 | 1296 | 4 | 1 | 1 | 0 | 2 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | ATGGC others(1291): Show |
chr17 | 30966039 | 31004911 | ||
| a0005c0005 | 0/0 | 1296 | 4 | 4 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | ATGGC others(1291): Show |
chr17 | 30966039 | 31004911 | ||
| a0006c0007 | 0/0 | 1296 | 3 | 3 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | ATGGC others(1291): Show |
chr17 | 30966039 | 31004911 | ||
| a0007c0008 | 0/0 | 1296 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | ATGGC others(1291): Show |
chr17 | 30966039 | 31004911 | ||
| a0008c0009 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | ATGGC others(1291): Show |
chr17 | 30966039 | 31004911 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2054 | 179 | 11 | 58 | 70 | 12 | 26 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0001c0001t0002 | 0/0 | 2054 | 2 | 2 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0001c0001t0006 | 0/0 | 2054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0002c0002t0001 | 0/0 | 2054 | 12 | 12 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0002c0002t0002 | 0/0 | 2054 | 40 | 34 | 6 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0002c0002t0003 | 0/0 | 2054 | 4 | 4 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0002c0002t0004 | 0/0 | 2054 | 5 | 3 | 2 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0002c0002t0007 | 0/0 | 2054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0002c0006t0001 | 0/0 | 2054 | 2 | 2 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0002c0006t0003 | 0/0 | 2054 | 2 | 2 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0003c0003t0001 | 0/0 | 2054 | 5 | 5 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0004c0004t0001 | 0/0 | 2054 | 4 | 1 | 1 | 0 | 2 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0005c0005t0001 | 0/0 | 2054 | 4 | 4 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0006c0007t0005 | 0/0 | 2045 | 3 | 3 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2040): Show |
chr17 | 30966039 | 31004911 |
| a0007c0008t0001 | 0/0 | 2054 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| a0008c0009t0003 | 0/0 | 2054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | AACCC others(2049): Show |
chr17 | 30966039 | 31004911 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0002t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0006t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0006t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0006t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0002c0006t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0003c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0003c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0004c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0004c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0004c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0004c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0005c0005t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0005c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0005c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0006c0007t0005g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0007c0008t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| a0008c0009t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00323 | hp1 | a0004 | c0004 | t0001 | g0091 | EUR | FIN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0038 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0051 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0052 | AMR | PUR | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01346 | hp1 | a0002 | c0002 | t0004 | g0244 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01433 | hp2 | a0002 | c0002 | t0004 | g0247 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01884 | hp1 | a0006 | c0007 | t0005 | g0001 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01943 | hp1 | a0007 | c0008 | t0001 | g0183 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01993 | hp2 | a0004 | c0004 | t0001 | g0092 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0050 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0070 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0058 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02280 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02615 | hp2 | a0006 | c0007 | t0005 | g0001 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02622 | hp1 | a0008 | c0009 | t0003 | g0025 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02630 | hp2 | a0004 | c0004 | t0001 | g0179 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0062 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02717 | hp2 | a0005 | c0005 | t0001 | g0005 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02809 | hp1 | a0002 | c0006 | t0003 | g0067 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0068 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0071 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02922 | hp2 | a0006 | c0007 | t0005 | g0001 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0060 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02970 | hp2 | a0005 | c0005 | t0001 | g0005 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0078 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0059 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0054 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03139 | hp2 | a0002 | c0002 | t0003 | g0075 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03209 | hp1 | a0002 | c0006 | t0003 | g0225 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03486 | hp1 | a0005 | c0005 | t0001 | g0023 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0246 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03516 | hp1 | a0002 | c0002 | t0007 | g0243 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ESN | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | GWD | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03579 | hp2 | a0002 | c0006 | t0001 | g0226 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | STU | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | YRI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | YRI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0245 | AFR | YRI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0041 | AFR | YRI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | LWK | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | LWK | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | LWK | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0047 | AFR | LWK | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | YRI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA19240 | hp2 | a0002 | c0002 | t0003 | g0031 | AFR | YRI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ASW | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0030 | AFR | ASW | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | TSI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20805 | hp2 | a0004 | c0004 | t0001 | g0090 | EUR | TSI | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | GIH | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0072 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02109 | hp2 | a0005 | c0005 | t0001 | g0022 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0065 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0064 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| HG03471 | hp2 | a0002 | c0006 | t0001 | g0227 | AFR | MSL | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | USA | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | USA | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| NA21309 | hp2 | a0002 | c0002 | t0004 | g0026 | AFR | LWK | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0109 | REF | REF | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0181 | REF | REF | RNF135_chr17_30966039_31004911 | RNF135 | chr17 | 30966039 | 31004911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30971286 | C | G | 4 | a0002 a0005 a0006 others(1): Show |
74 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(71): Show |
missense_variant | MODERATE | c.213C>G | p.His71Gln | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/5 | 248/2054 | 213/1299 | 71/432 | chr17 | 30971286 | |||
| chr17:30971365 | C | G | 1 | a0005 | 4 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
missense_variant | MODERATE | c.292C>G | p.Pro98Ala | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/5 | 327/2054 | 292/1299 | 98/432 | chr17 | 30971365 | |||
| chr17:30971395 | T | C | 4 | a0002 a0003 a0005 others(1): Show |
76 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(73): Show |
missense_variant | MODERATE | c.322T>C | p.Ser108Pro | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/5 | 357/2054 | 322/1299 | 108/432 | chr17 | 30971395 | |||
| chr17:30971417 | G | A | 1 | a0004 | 4 | HG00323.hp1 HG01993.hp2 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.344G>A | p.Arg115Lys | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/5 | 379/2054 | 344/1299 | 115/432 | chr17 | 30971417 | |||
| chr17:30988020 | G | A | 1 | a0007 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.593G>A | p.Arg198Lys | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/5 | 628/2054 | 593/1299 | 198/432 | chr17 | 30988020 | |||
| chr17:30998686 | T | G | 1 | a0008 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.794T>G | p.Leu265Trp | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 5/5 | 829/2054 | 794/1299 | 265/432 | chr17 | 30998686 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30971202 | C | T | 1 | a0002c0006 | 4 | HG02809.hp1 HG03209.hp1 HG03471.hp2 others(1): Show |
synonymous_variant | LOW | c.129C>T | p.His43His | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/5 | 164/2054 | 129/1299 | 43/432 | chr17 | 30971202 | |||
| chr17:30971433 | G | T | 4 | a0002c0002 a0005c0005 a0006c0007 others(1): Show |
70 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(67): Show |
synonymous_variant | LOW | c.360G>T | p.Pro120Pro | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/5 | 395/2054 | 360/1299 | 120/432 | chr17 | 30971433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30971046 | ACGTCCGC others(2): Show |
A | 1 | a0006c0007t0005 | 3 | HG01884.hp1 HG02615.hp2 HG02922.hp2 |
5_prime_UTR_variant | MODIFIER | c.-26_-18delGTCCGCGC others(1): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/5 | 18 | INFO_REALIGN_3_PRIME | chr17 | 30971046 | |||||
| chr17:30999246 | A | C | 1 | a0002c0002t0007 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*55A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 5/5 | 55 | chr17 | 30999246 | ||||||
| chr17:30999293 | C | T | 1 | a0001c0001t0006 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*102C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 5/5 | 102 | chr17 | 30999293 | ||||||
| chr17:30999483 | C | T | 3 | a0001c0001t0002 a0002c0002t0002 a0006c0007t0005 |
45 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*292C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 5/5 | 292 | chr17 | 30999483 | ||||||
| chr17:30999628 | G | A | 3 | a0002c0002t0003 a0002c0006t0003 a0008c0009t0003 |
7 | HG02280.hp2 HG02622.hp1 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 5/5 | 437 | chr17 | 30999628 | ||||||
| chr17:30999717 | C | G | 5 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0004 others(2): Show |
51 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*526C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 5/5 | 526 | chr17 | 30999717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30971587 | C | T | 5 | a0002c0002t0004g0244 a0002c0002t0004g0245 a0002c0002t0004g0246 others(2): Show |
5 | HG01346.hp1 HG01433.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+142C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30971587 | |||||||
| chr17:30971891 | G | A | 63 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(60): Show |
70 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.372+446G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30971891 | |||||||
| chr17:30972289 | T | A | 6 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(3): Show |
7 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+844T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30972289 | |||||||
| chr17:30972293 | A | T | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.372+848A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30972293 | |||||||
| chr17:30972490 | C | G | 1 | a0002c0002t0002g0068 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.372+1045C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30972490 | |||||||
| chr17:30972499 | T | G | 1 | a0001c0001t0001g0009 | 2 | NA18956.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.372+1054T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30972499 | |||||||
| chr17:30972529 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.372+1084C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30972529 | |||||||
| chr17:30972564 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.372+1119G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30972564 | |||||||
| chr17:30972637 | T | C | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1192T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30972637 | |||||||
| chr17:30972790 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.372+1345G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30972790 | |||||||
| chr17:30973054 | G | A | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1609G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30973054 | |||||||
| chr17:30973071 | G | A | 3 | a0005c0005t0001g0005 a0005c0005t0001g0022 a0005c0005t0001g0023 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+1626G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30973071 | |||||||
| chr17:30973225 | G | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.372+1780G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30973225 | |||||||
| chr17:30973269 | T | A | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.372+1824T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30973269 | |||||||
| chr17:30973403 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.372+1958T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30973403 | |||||||
| chr17:30973472 | GT | G | 63 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(60): Show |
70 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.372+2040delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30973472 | ||||||
| chr17:30973555 | C | T | 6 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(3): Show |
6 | HG00741.hp1 HG01099.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+2110C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30973555 | |||||||
| chr17:30973568 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.372+2123A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30973568 | |||||||
| chr17:30973692 | C | T | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.372+2247C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30973692 | |||||||
| chr17:30974023 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.372+2578A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974023 | |||||||
| chr17:30974100 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.372+2655A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974100 | |||||||
| chr17:30974153 | G | A | 2 | a0002c0002t0001g0027 a0002c0002t0004g0026 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.372+2708G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974153 | |||||||
| chr17:30974182 | T | A | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.372+2737T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974182 | |||||||
| chr17:30974200 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.372+2755T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974200 | |||||||
| chr17:30974205 | A | G | 7 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(4): Show |
8 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.372+2760A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974205 | |||||||
| chr17:30974267 | C | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.372+2822C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974267 | |||||||
| chr17:30974342 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.372+2897G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974342 | |||||||
| chr17:30974363 | T | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0006g0078 |
3 | HG00735.hp2 HG01081.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.372+2918T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974363 | |||||||
| chr17:30974590 | A | AT | 7 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
8 | HG02109.hp1 HG02135.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.372+3156dupT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30974590 | ||||||
| chr17:30974590 | AT | A | 9 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(6): Show |
10 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.372+3156delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30974590 | ||||||
| chr17:30974601 | T | G | 1 | a0002c0002t0002g0028 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.372+3156T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974601 | |||||||
| chr17:30974687 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.372+3242T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974687 | |||||||
| chr17:30974688 | A | T | 13 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(10): Show |
14 | HG00423.hp2 HG01978.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.372+3243A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974688 | |||||||
| chr17:30974691 | T | A | 66 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0002c0002t0001g0004 others(63): Show |
73 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.372+3246T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974691 | |||||||
| chr17:30974728 | G | A | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.372+3283G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974728 | |||||||
| chr17:30974794 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.372+3349C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974794 | |||||||
| chr17:30974804 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | NA19011.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.372+3359C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974804 | |||||||
| chr17:30974805 | G | A | 55 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(52): Show |
61 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.372+3360G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974805 | |||||||
| chr17:30974883 | A | G | 68 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(65): Show |
76 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(73): Show |
intron_variant | MODIFIER | c.372+3438A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974883 | |||||||
| chr17:30974948 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.372+3503G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30974948 | |||||||
| chr17:30975032 | C | T | 68 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(65): Show |
76 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(73): Show |
intron_variant | MODIFIER | c.372+3587C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30975032 | |||||||
| chr17:30975211 | T | A | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.372+3766T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30975211 | |||||||
| chr17:30975217 | C | T | 8 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(5): Show |
9 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.372+3772C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30975217 | |||||||
| chr17:30975537 | C | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.372+4092C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30975537 | |||||||
| chr17:30975794 | A | G | 9 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(6): Show |
10 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.372+4349A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30975794 | |||||||
| chr17:30975988 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.372+4543A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30975988 | |||||||
| chr17:30975989 | AT | A | 52 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(49): Show |
58 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.372+4545delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30975989 | |||||||
| chr17:30976067 | G | A | 1 | a0002c0002t0002g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.372+4622G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30976067 | |||||||
| chr17:30976195 | G | A | 3 | a0005c0005t0001g0005 a0005c0005t0001g0022 a0005c0005t0001g0023 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+4750G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30976195 | |||||||
| chr17:30976432 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.372+4987G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30976432 | |||||||
| chr17:30976550 | T | G | 1 | a0002c0002t0001g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.372+5105T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30976550 | |||||||
| chr17:30976562 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.372+5117C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30976562 | |||||||
| chr17:30976610 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.372+5165T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30976610 | |||||||
| chr17:30976806 | C | G | 1 | a0002c0002t0002g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.372+5361C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30976806 | |||||||
| chr17:30976933 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.372+5488C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30976933 | |||||||
| chr17:30976965 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.372+5520T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30976965 | |||||||
| chr17:30977218 | GAAAACTA others(3): Show |
G | 1 | a0001c0001t0002g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.372+5780_372+5789d others(12): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30977218 | ||||||
| chr17:30977348 | C | T | 55 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(52): Show |
61 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.372+5903C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30977348 | |||||||
| chr17:30977510 | A | G | 2 | a0002c0002t0004g0246 a0002c0002t0004g0247 |
2 | HG01433.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.372+6065A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30977510 | |||||||
| chr17:30977537 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.372+6092C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30977537 | |||||||
| chr17:30977795 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | NA18941.hp1 NA18984.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.372+6350C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30977795 | |||||||
| chr17:30977860 | C | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.372+6415C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30977860 | |||||||
| chr17:30978054 | G | A | 1 | a0002c0002t0004g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.373-6563G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978054 | |||||||
| chr17:30978141 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.373-6476C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978141 | |||||||
| chr17:30978231 | C | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-6386C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978231 | |||||||
| chr17:30978288 | A | G | 3 | a0002c0002t0002g0060 a0002c0002t0002g0061 a0002c0002t0002g0062 |
3 | HG02717.hp1 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.373-6329A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978288 | |||||||
| chr17:30978307 | C | A | 1 | a0002c0002t0002g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.373-6310C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978307 | |||||||
| chr17:30978520 | C | G | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.373-6097C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978520 | |||||||
| chr17:30978551 | C | T | 71 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(68): Show |
79 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.373-6066C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978551 | |||||||
| chr17:30978601 | TA | T | 6 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0004g0026 others(3): Show |
7 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.373-6015delA | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978601 | |||||||
| chr17:30978602 | A | T | 59 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(56): Show |
66 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.373-6015A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978602 | |||||||
| chr17:30978603 | T | A | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-6014T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978603 | |||||||
| chr17:30978616 | A | AT | 8 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(5): Show |
9 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-5991dupT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30978616 | ||||||
| chr17:30978616 | AT | A | 5 | a0002c0002t0004g0244 a0002c0002t0004g0245 a0002c0002t0004g0246 others(2): Show |
5 | HG01346.hp1 HG01433.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-5991delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30978616 | ||||||
| chr17:30978957 | A | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.373-5660A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978957 | |||||||
| chr17:30978996 | C | A | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-5621C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30978996 | |||||||
| chr17:30979017 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.373-5600A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979017 | |||||||
| chr17:30979061 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.373-5556C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979061 | |||||||
| chr17:30979083 | C | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0080 others(8): Show |
11 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.373-5534C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979083 | |||||||
| chr17:30979084 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.373-5533G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979084 | |||||||
| chr17:30979110 | A | G | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.373-5507A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979110 | |||||||
| chr17:30979110 | A | T | 3 | a0002c0002t0001g0004 a0002c0002t0001g0020 a0002c0002t0001g0021 |
4 | HG02145.hp2 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-5507A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979110 | |||||||
| chr17:30979116 | T | C | 9 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(6): Show |
10 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-5501T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979116 | |||||||
| chr17:30979134 | G | C | 55 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(52): Show |
61 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.373-5483G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979134 | |||||||
| chr17:30979148 | C | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-5469C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979148 | |||||||
| chr17:30979149 | GGGCAGAG others(121): Show |
G | 3 | a0005c0005t0001g0005 a0005c0005t0001g0022 a0005c0005t0001g0023 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-5424_373-5297d others(2): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979149 | ||||||
| chr17:30979236 | G | C | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.373-5381G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979236 | |||||||
| chr17:30979237 | C | G | 1 | a0001c0001t0002g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.373-5380C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979237 | |||||||
| chr17:30979240 | A | AC | 61 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(58): Show |
62 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.373-5366dupC | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979240 | ||||||
| chr17:30979240 | A | ACC | 31 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0002c0002t0001g0004 others(28): Show |
34 | HG01069.hp1 HG01071.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.373-5367_373-5366d others(4): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979240 | ||||||
| chr17:30979240 | A | ACCC | 13 | a0002c0002t0001g0018 a0002c0002t0002g0030 a0002c0002t0002g0033 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.373-5368_373-5366d others(5): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979240 | ||||||
| chr17:30979243 | C | A | 1 | a0001c0001t0001g0200 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.373-5374C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979243 | |||||||
| chr17:30979258 | C | T | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-5359C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979258 | |||||||
| chr17:30979295 | C | G | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-5322C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979295 | |||||||
| chr17:30979310 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.373-5307G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979310 | |||||||
| chr17:30979346 | C | T | 3 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0002c0006t0003g0225 |
3 | HG03209.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.373-5271C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979346 | |||||||
| chr17:30979373 | C | T | 10 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(7): Show |
10 | HG00438.hp1 HG01167.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-5244C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979373 | |||||||
| chr17:30979375 | C | T | 41 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0057 others(38): Show |
46 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.373-5242C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979375 | |||||||
| chr17:30979476 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.373-5141C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979476 | |||||||
| chr17:30979512 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.373-5105C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979512 | |||||||
| chr17:30979514 | G | A | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-5103G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979514 | |||||||
| chr17:30979532 | A | AC | 70 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0073 others(67): Show |
74 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.373-5073dupC | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979532 | ||||||
| chr17:30979532 | A | ACC | 67 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0013 others(64): Show |
72 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.373-5074_373-5073d others(4): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979532 | ||||||
| chr17:30979532 | A | ACCC | 18 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0069 others(15): Show |
21 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.373-5075_373-5073d others(5): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979532 | ||||||
| chr17:30979532 | A | ACCCC | 19 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0089 others(16): Show |
20 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.373-5076_373-5073d others(6): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979532 | ||||||
| chr17:30979532 | AC | A | 27 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0002g0006 others(24): Show |
31 | HG00738.hp1 HG01071.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.373-5073delC | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979532 | ||||||
| chr17:30979532 | ACC | A | 14 | a0002c0002t0001g0057 a0002c0002t0002g0008 a0002c0002t0002g0030 others(11): Show |
15 | HG01069.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.373-5074_373-5073d others(4): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979532 | ||||||
| chr17:30979532 | ACCCCCCC others(6): Show |
A | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-5082_373-5070d others(15): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979532 | ||||||
| chr17:30979536 | C | G | 1 | a0002c0002t0002g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.373-5081C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979536 | |||||||
| chr17:30979537 | C | CT | 3 | a0005c0005t0001g0005 a0005c0005t0001g0022 a0005c0005t0001g0023 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-5080_373-5079i others(3): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979537 | |||||||
| chr17:30979542 | C | A | 3 | a0005c0005t0001g0005 a0005c0005t0001g0022 a0005c0005t0001g0023 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-5075C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979542 | |||||||
| chr17:30979545 | G | A | 5 | a0002c0002t0002g0028 a0002c0002t0002g0032 a0002c0002t0002g0033 others(2): Show |
5 | HG02258.hp1 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-5072G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979545 | |||||||
| chr17:30979651 | AGGCGGGG others(43): Show |
A | 2 | a0002c0002t0001g0027 a0002c0002t0004g0026 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.373-4952_373-4903d others(52): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979651 | ||||||
| chr17:30979659 | G | T | 1 | a0002c0002t0002g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.373-4958G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979659 | |||||||
| chr17:30979664 | ATCCCCCC others(42): Show |
A | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.373-4952_373-4904d others(51): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979664 | |||||||
| chr17:30979670 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.373-4947C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979670 | |||||||
| chr17:30979676 | TCCCTCCC others(91): Show |
T | 1 | a0004c0004t0001g0090 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.373-4895_373-4798d others(100): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979676 | ||||||
| chr17:30979705 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.373-4912G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979705 | |||||||
| chr17:30979714 | A | AC | 24 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0101 others(21): Show |
25 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.373-4895dupC | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30979714 | ||||||
| chr17:30979714 | A | C | 2 | a0001c0001t0001g0113 a0002c0002t0001g0065 |
2 | HG02559.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.373-4903A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979714 | |||||||
| chr17:30979771 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.373-4846T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979771 | |||||||
| chr17:30979775 | C | A | 1 | a0002c0002t0004g0246 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.373-4842C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979775 | |||||||
| chr17:30979777 | C | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-4840C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979777 | |||||||
| chr17:30979781 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.373-4836C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979781 | |||||||
| chr17:30979864 | C | T | 8 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(5): Show |
9 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-4753C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979864 | |||||||
| chr17:30979880 | C | T | 8 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(5): Show |
9 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-4737C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979880 | |||||||
| chr17:30979883 | G | A | 8 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(5): Show |
9 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-4734G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979883 | |||||||
| chr17:30979891 | G | A | 8 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(5): Show |
9 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-4726G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979891 | |||||||
| chr17:30979920 | C | T | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-4697C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979920 | |||||||
| chr17:30979937 | G | A | 6 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0004g0026 others(3): Show |
7 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.373-4680G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979937 | |||||||
| chr17:30979962 | C | T | 3 | a0005c0005t0001g0005 a0005c0005t0001g0022 a0005c0005t0001g0023 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-4655C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979962 | |||||||
| chr17:30979999 | C | G | 1 | a0002c0002t0004g0245 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.373-4618C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30979999 | |||||||
| chr17:30980009 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.373-4608G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980009 | |||||||
| chr17:30980025 | GGGCGGGG others(41): Show |
G | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-4577_373-4530d others(50): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30980025 | ||||||
| chr17:30980039 | CCCCCCAC others(42): Show |
C | 8 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(5): Show |
9 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-4562_373-4514d others(51): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30980039 | ||||||
| chr17:30980073 | A | G | 56 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(53): Show |
62 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.373-4544A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980073 | |||||||
| chr17:30980115 | ACTGGCCG others(120): Show |
A | 1 | a0001c0001t0001g0215 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.373-4484_373-4358d others(2): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30980115 | ||||||
| chr17:30980127 | G | A | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.373-4490G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980127 | |||||||
| chr17:30980133 | CTCCTCAC others(119): Show |
C | 1 | a0001c0001t0001g0239 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.373-4459_373-4334d others(2): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30980133 | ||||||
| chr17:30980220 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.373-4397C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980220 | |||||||
| chr17:30980337 | T | C | 5 | a0002c0002t0004g0244 a0002c0002t0004g0245 a0002c0002t0004g0246 others(2): Show |
5 | HG01346.hp1 HG01433.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-4280T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980337 | |||||||
| chr17:30980375 | G | C | 4 | a0004c0004t0001g0090 a0004c0004t0001g0091 a0004c0004t0001g0092 others(1): Show |
4 | HG00323.hp1 HG01993.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-4242G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980375 | |||||||
| chr17:30980380 | G | C | 3 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0002c0006t0003g0225 |
3 | HG03209.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.373-4237G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980380 | |||||||
| chr17:30980395 | T | G | 3 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0002c0006t0003g0225 |
3 | HG03209.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.373-4222T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980395 | |||||||
| chr17:30980448 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.373-4169C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980448 | |||||||
| chr17:30980493 | C | A | 55 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(52): Show |
61 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.373-4124C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980493 | |||||||
| chr17:30980504 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.373-4113C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980504 | |||||||
| chr17:30980526 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.373-4091C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980526 | |||||||
| chr17:30980587 | G | A | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-4030G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980587 | |||||||
| chr17:30980647 | G | C | 6 | a0002c0002t0002g0006 a0002c0002t0002g0035 a0002c0002t0002g0050 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-3970G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980647 | |||||||
| chr17:30980656 | G | A | 50 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(47): Show |
56 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.373-3961G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980656 | |||||||
| chr17:30980767 | C | T | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.373-3850C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980767 | |||||||
| chr17:30980842 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.373-3775G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980842 | |||||||
| chr17:30980861 | C | T | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.373-3756C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980861 | |||||||
| chr17:30980874 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.373-3743C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980874 | |||||||
| chr17:30980905 | C | T | 8 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(5): Show |
9 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-3712C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980905 | |||||||
| chr17:30980932 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.373-3685A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980932 | |||||||
| chr17:30980961 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.373-3656G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30980961 | |||||||
| chr17:30981044 | C | T | 3 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0002c0006t0003g0225 |
3 | HG03209.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.373-3573C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981044 | |||||||
| chr17:30981070 | A | C | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.373-3547A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981070 | |||||||
| chr17:30981087 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.373-3530C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981087 | |||||||
| chr17:30981088 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.373-3529G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981088 | |||||||
| chr17:30981166 | C | T | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0239 |
3 | HG01261.hp2 HG01358.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.373-3451C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981166 | |||||||
| chr17:30981177 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0116 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.373-3440G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981177 | |||||||
| chr17:30981187 | G | A | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.373-3430G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981187 | |||||||
| chr17:30981195 | C | CA | 21 | a0001c0001t0001g0069 a0001c0001t0001g0103 a0001c0001t0001g0112 others(18): Show |
21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.373-3413dupA | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30981195 | ||||||
| chr17:30981229 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.373-3388G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981229 | |||||||
| chr17:30981232 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.373-3385C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981232 | |||||||
| chr17:30981243 | G | A | 1 | a0002c0006t0003g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.373-3374G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981243 | |||||||
| chr17:30981254 | A | G | 72 | a0001c0001t0001g0233 a0002c0002t0001g0004 a0002c0002t0001g0017 others(69): Show |
80 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(77): Show |
intron_variant | MODIFIER | c.373-3363A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981254 | |||||||
| chr17:30981329 | C | G | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.373-3288C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981329 | |||||||
| chr17:30981330 | A | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(115): Show |
132 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(129): Show |
intron_variant | MODIFIER | c.373-3287A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981330 | |||||||
| chr17:30981333 | A | G | 3 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0057 |
3 | HG02965.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.373-3284A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981333 | |||||||
| chr17:30981347 | G | A | 55 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(52): Show |
61 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.373-3270G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981347 | |||||||
| chr17:30981349 | G | GGAGGCA | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-3264_373-3263i others(8): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30981349 | ||||||
| chr17:30981349 | G | GGAGGGA | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(228): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.373-3246_373-3241d others(8): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30981349 | ||||||
| chr17:30981349 | G | GGAGGGAG others(5): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0002c0002t0002g0063 |
3 | HG01167.hp1 HG01192.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.373-3252_373-3241d others(14): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30981349 | ||||||
| chr17:30981471 | G | T | 64 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(61): Show |
71 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.373-3146G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981471 | |||||||
| chr17:30981896 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.373-2721A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981896 | |||||||
| chr17:30981993 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.373-2624A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30981993 | |||||||
| chr17:30982036 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.373-2581C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982036 | |||||||
| chr17:30982156 | C | G | 8 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(5): Show |
9 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-2461C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982156 | |||||||
| chr17:30982254 | C | T | 1 | a0002c0002t0002g0034 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.373-2363C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982254 | |||||||
| chr17:30982313 | G | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-2304G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982313 | |||||||
| chr17:30982397 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(185): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.373-2220C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982397 | |||||||
| chr17:30982399 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.373-2218A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982399 | |||||||
| chr17:30982451 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.373-2166T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982451 | |||||||
| chr17:30982497 | T | C | 55 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(52): Show |
61 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.373-2120T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982497 | |||||||
| chr17:30982507 | A | G | 2 | a0002c0002t0002g0060 a0002c0002t0002g0062 |
2 | HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.373-2110A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982507 | |||||||
| chr17:30982758 | C | T | 5 | a0002c0002t0004g0244 a0002c0002t0004g0245 a0002c0002t0004g0246 others(2): Show |
5 | HG01346.hp1 HG01433.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-1859C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30982758 | |||||||
| chr17:30983258 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0167 |
2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.373-1359A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983258 | |||||||
| chr17:30983307 | TTACATAT others(3): Show |
T | 3 | a0005c0005t0001g0005 a0005c0005t0001g0022 a0005c0005t0001g0023 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1300_373-1291d others(12): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983307 | ||||||
| chr17:30983317 | G | A | 3 | a0002c0002t0001g0027 a0002c0002t0003g0024 a0008c0009t0003g0025 |
3 | HG02257.hp1 HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.373-1300G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983317 | |||||||
| chr17:30983320 | C | CATAT | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0089 others(4): Show |
7 | HG00140.hp2 HG00735.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.373-1266_373-1263d others(6): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | C | CATATAT | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0159 others(1): Show |
4 | HG01123.hp2 NA18944.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1268_373-1263d others(8): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | C | CATATATA others(1): Show |
3 | a0001c0001t0001g0077 a0001c0001t0001g0095 a0004c0004t0001g0092 |
3 | HG00642.hp1 HG01993.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.373-1270_373-1263d others(10): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | C | CATATATA others(3): Show |
10 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0001g0105 others(7): Show |
10 | HG00323.hp1 HG01243.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-1272_373-1263d others(12): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | C | CATATATA others(5): Show |
14 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0001g0106 others(11): Show |
14 | HG01069.hp2 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.373-1274_373-1263d others(14): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | C | CATATATA others(7): Show |
7 | a0001c0001t0001g0094 a0001c0001t0001g0108 a0001c0001t0001g0158 others(4): Show |
7 | HG01071.hp1 HG01258.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.373-1276_373-1263d others(16): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | C | CATATATA others(9): Show |
9 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0118 others(6): Show |
9 | HG00140.hp1 HG01261.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.373-1278_373-1263d others(18): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | C | CATATATA others(11): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0149 others(2): Show |
6 | HG00280.hp1 HG00280.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-1280_373-1263d others(20): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | C | CATATATA others(13): Show |
6 | a0001c0001t0001g0104 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG01123.hp1 HG01175.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-1282_373-1263d others(22): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | C | CATATATA others(15): Show |
1 | a0001c0001t0001g0207 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.373-1284_373-1263d others(24): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | CATATAT | C | 5 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0116 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-1268_373-1263d others(8): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | CATATATA others(3): Show |
C | 7 | a0001c0001t0001g0238 a0002c0002t0001g0017 a0002c0002t0002g0007 others(4): Show |
9 | HG00741.hp1 HG02723.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-1272_373-1263d others(12): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | CATATATA others(5): Show |
C | 12 | a0001c0001t0001g0174 a0002c0002t0001g0004 a0002c0002t0001g0018 others(9): Show |
13 | HG01346.hp1 HG01433.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.373-1274_373-1263d others(14): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983320 | CATATATA others(13): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.373-1282_373-1263d others(22): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983320 | ||||||
| chr17:30983326 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.373-1291T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983326 | |||||||
| chr17:30983328 | T | C | 1 | a0002c0002t0004g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.373-1289T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983328 | |||||||
| chr17:30983330 | T | C | 3 | a0005c0005t0001g0005 a0005c0005t0001g0022 a0005c0005t0001g0023 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1287T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983330 | |||||||
| chr17:30983332 | TATATATA others(14): Show |
T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-1284_373-1264d others(23): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983332 | |||||||
| chr17:30983335 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0119 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.373-1280_373-1261d others(22): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983335 | ||||||
| chr17:30983337 | ATATATAT others(13): Show |
A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | HG00423.hp1 HG02015.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1278_373-1259d others(22): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983337 | ||||||
| chr17:30983340 | TATATATA | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0073 others(7): Show |
11 | HG00438.hp1 HG01978.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.373-1276_373-1270d others(9): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983340 | |||||||
| chr17:30983341 | ATATATAT others(7): Show |
A | 1 | a0002c0002t0003g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.373-1274_373-1261d others(16): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983341 | ||||||
| chr17:30983341 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0164 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.373-1274_373-1259d others(18): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983341 | ||||||
| chr17:30983342 | TATATATA | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(22): Show |
28 | HG00639.hp2 HG00642.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.373-1274_373-1268d others(9): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983342 | |||||||
| chr17:30983343 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.373-1274A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983343 | |||||||
| chr17:30983343 | ATATATAT others(4): Show |
A | 1 | a0002c0002t0002g0055 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.373-1272_373-1262d others(13): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983343 | ||||||
| chr17:30983343 | ATATATAT others(5): Show |
A | 1 | a0002c0002t0003g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.373-1272_373-1261d others(14): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983343 | ||||||
| chr17:30983345 | A | T | 3 | a0001c0001t0001g0233 a0002c0002t0001g0027 a0002c0002t0004g0026 |
3 | HG02257.hp1 HG03490.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.373-1272A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983345 | |||||||
| chr17:30983345 | ATATATAT others(3): Show |
A | 8 | a0002c0002t0002g0029 a0002c0002t0002g0030 a0002c0002t0002g0041 others(5): Show |
10 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-1270_373-1261d others(12): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983345 | ||||||
| chr17:30983347 | A | ATTTTTTT others(5): Show |
1 | a0003c0003t0001g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-1269_373-1268i others(14): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983347 | ||||||
| chr17:30983347 | A | T | 9 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0102 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.373-1270A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983347 | |||||||
| chr17:30983347 | ATATATAT others(2): Show |
A | 6 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0057 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-1268_373-1260d others(11): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983347 | ||||||
| chr17:30983347 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0014 a0002c0002t0002g0060 |
2 | HG01074.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.373-1268_373-1259d others(12): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983347 | ||||||
| chr17:30983349 | A | T | 27 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0073 others(24): Show |
28 | HG00438.hp1 HG01346.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.373-1268A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983349 | |||||||
| chr17:30983349 | ATATATT | A | 5 | a0001c0001t0001g0184 a0002c0002t0002g0006 a0002c0002t0002g0036 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-1266_373-1261d others(8): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983349 | ||||||
| chr17:30983351 | A | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(53): Show |
62 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.373-1266A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983351 | |||||||
| chr17:30983351 | ATATTTT | A | 5 | a0002c0002t0002g0006 a0002c0002t0002g0035 a0002c0002t0002g0046 others(2): Show |
5 | HG01243.hp2 HG02055.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-1264_373-1259d others(8): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983351 | ||||||
| chr17:30983353 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.373-1263_373-1262i others(13): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG02135.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.373-1263_373-1262i others(23): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0002 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.373-1263_373-1262i others(20): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.373-1263_373-1262i others(22): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0127 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.373-1263_373-1262i others(20): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.373-1263_373-1262i others(21): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0206 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.373-1263_373-1262i others(22): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0172 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.373-1263_373-1262i others(23): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0223 a0001c0001t0001g0234 |
3 | HG00423.hp2 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.373-1263_373-1262i others(16): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0129 |
2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.373-1263_373-1262i others(18): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.373-1263_373-1262i others(21): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(33): Show |
1 | a0003c0003t0001g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.373-1263_373-1262i others(42): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0015 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.373-1263_373-1262i others(14): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0237 |
2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.373-1263_373-1262i others(15): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.373-1263_373-1262i others(20): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0120 a0001c0001t0001g0171 a0004c0004t0001g0179 |
3 | HG00408.hp2 HG02630.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.373-1263_373-1262i others(12): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0081 a0001c0001t0001g0114 |
2 | HG01192.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.373-1263_373-1262i others(14): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0117 |
2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.373-1263_373-1262i others(13): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATATATTT others(11): Show |
2 | a0003c0003t0001g0010 a0003c0003t0001g0071 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.373-1263_373-1262i others(20): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATTTTTTT others(8): Show |
1 | a0002c0006t0003g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.373-1260_373-1246d others(17): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | ATTTTTTT others(31): Show |
1 | a0003c0003t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.373-1246_373-1245i others(40): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983353 | ||||||
| chr17:30983353 | A | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(66): Show |
76 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.373-1264A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983353 | |||||||
| chr17:30983354 | T | TATATATA others(4): Show |
5 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0147 others(2): Show |
5 | HG01255.hp2 HG01433.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-1263_373-1262i others(13): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983354 | |||||||
| chr17:30983354 | T | TATATATA others(6): Show |
5 | a0001c0001t0001g0107 a0001c0001t0001g0123 a0001c0001t0001g0146 others(2): Show |
5 | HG00323.hp2 HG00438.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-1263_373-1262i others(15): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983354 | |||||||
| chr17:30983354 | T | TATATATA others(12): Show |
1 | a0001c0001t0001g0150 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.373-1263_373-1262i others(21): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983354 | |||||||
| chr17:30983354 | T | TATATATA others(14): Show |
1 | a0001c0001t0006g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.373-1263_373-1262i others(23): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983354 | |||||||
| chr17:30983355 | T | A | 54 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0077 others(51): Show |
55 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.373-1262T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983355 | |||||||
| chr17:30983356 | T | A | 4 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0178 others(1): Show |
4 | HG00438.hp2 HG01433.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1261T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983356 | |||||||
| chr17:30983357 | T | A | 17 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0103 others(14): Show |
18 | HG00280.hp2 HG01109.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.373-1260T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983357 | |||||||
| chr17:30983358 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0178 |
2 | HG00438.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.373-1259T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983358 | |||||||
| chr17:30983359 | T | A | 5 | a0001c0001t0001g0069 a0001c0001t0001g0105 a0001c0001t0001g0144 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-1258T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983359 | |||||||
| chr17:30983361 | T | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0105 |
2 | HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.373-1256T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983361 | |||||||
| chr17:30983363 | T | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0105 |
2 | HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.373-1254T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983363 | |||||||
| chr17:30983393 | G | A | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-1224G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983393 | |||||||
| chr17:30983415 | A | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373-1202A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983415 | |||||||
| chr17:30983560 | G | T | 55 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(52): Show |
61 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.373-1057G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983560 | |||||||
| chr17:30983573 | C | T | 1 | a0002c0002t0003g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.373-1044C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983573 | |||||||
| chr17:30983600 | C | T | 3 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0004g0026 |
3 | HG02257.hp1 HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.373-1017C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983600 | |||||||
| chr17:30983766 | G | GT | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0195 others(2): Show |
5 | HG02630.hp1 HG02738.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-838dupT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 30983766 | ||||||
| chr17:30983821 | T | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0164 a0001c0001t0001g0242 |
3 | HG00738.hp2 HG01358.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.373-796T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983821 | |||||||
| chr17:30983934 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.373-683T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983934 | |||||||
| chr17:30983976 | A | G | 2 | a0002c0002t0003g0031 a0002c0002t0003g0075 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.373-641A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30983976 | |||||||
| chr17:30984331 | A | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.373-286A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 1/4 | chr17 | 30984331 | |||||||
| chr17:30984938 | G | C | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+178G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30984938 | |||||||
| chr17:30985159 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.516+399C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30985159 | |||||||
| chr17:30985482 | C | T | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.516+722C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30985482 | |||||||
| chr17:30985522 | TG | T | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+763delG | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30985522 | |||||||
| chr17:30985528 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.516+768T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30985528 | |||||||
| chr17:30985686 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.516+926C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30985686 | |||||||
| chr17:30985696 | A | ACTACCAC others(24): Show |
1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516+938_516+968dup others(31): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 30985696 | ||||||
| chr17:30985853 | T | C | 58 | a0002c0002t0001g0027 a0002c0002t0001g0048 a0002c0002t0001g0049 others(55): Show |
64 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.516+1093T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30985853 | |||||||
| chr17:30985885 | C | T | 3 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0002c0006t0003g0225 |
3 | HG03209.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.516+1125C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30985885 | |||||||
| chr17:30986060 | A | G | 55 | a0002c0002t0001g0004 a0002c0002t0001g0017 a0002c0002t0001g0018 others(52): Show |
61 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.516+1300A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30986060 | |||||||
| chr17:30986215 | C | CT | 6 | a0001c0001t0001g0102 a0001c0001t0001g0185 a0002c0002t0001g0065 others(3): Show |
6 | HG01175.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+1468dupT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 30986215 | ||||||
| chr17:30986257 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.516+1497C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30986257 | |||||||
| chr17:30986282 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.516+1522C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30986282 | |||||||
| chr17:30986365 | T | A | 13 | a0002c0002t0001g0065 a0002c0002t0003g0024 a0002c0006t0001g0226 others(10): Show |
15 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.517-1579T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30986365 | |||||||
| chr17:30986446 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | NA19011.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.517-1498C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30986446 | |||||||
| chr17:30986589 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.517-1355A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30986589 | |||||||
| chr17:30986670 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.517-1274T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30986670 | |||||||
| chr17:30986894 | C | T | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.517-1050C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30986894 | |||||||
| chr17:30986981 | C | G | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517-963C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30986981 | |||||||
| chr17:30987172 | A | G | 5 | a0002c0002t0004g0244 a0002c0002t0004g0245 a0002c0002t0004g0246 others(2): Show |
5 | HG01346.hp1 HG01433.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-772A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30987172 | |||||||
| chr17:30987231 | CT | C | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-700delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 30987231 | ||||||
| chr17:30987502 | G | T | 49 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0057 others(46): Show |
54 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.517-442G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30987502 | |||||||
| chr17:30987766 | TACAGCAA | T | 65 | a0002c0002t0001g0027 a0002c0002t0001g0048 a0002c0002t0001g0049 others(62): Show |
72 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(69): Show |
intron_variant | MODIFIER | c.517-176_517-170del others(7): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 30987766 | ||||||
| chr17:30987821 | G | A | 1 | a0002c0002t0003g0064 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.517-123G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 2/4 | chr17 | 30987821 | |||||||
| chr17:30988175 | G | C | 49 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0057 others(46): Show |
54 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.679+69G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988175 | |||||||
| chr17:30988255 | A | G | 2 | a0002c0002t0004g0246 a0002c0002t0004g0247 |
2 | HG01433.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.679+149A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988255 | |||||||
| chr17:30988258 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.679+152T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988258 | |||||||
| chr17:30988387 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.679+281T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988387 | |||||||
| chr17:30988397 | C | G | 3 | a0002c0002t0002g0037 a0002c0002t0002g0045 a0002c0002t0002g0059 |
3 | HG02486.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.679+291C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988397 | |||||||
| chr17:30988407 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.679+301C>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988407 | |||||||
| chr17:30988416 | A | AT | 83 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
89 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.679+339dupT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30988416 | ||||||
| chr17:30988416 | A | ATT | 12 | a0001c0001t0001g0151 a0001c0001t0001g0202 a0001c0001t0001g0242 others(9): Show |
13 | HG00738.hp2 HG01346.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.679+338_679+339dup others(2): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30988416 | ||||||
| chr17:30988416 | AT | A | 9 | a0001c0001t0001g0069 a0001c0001t0001g0208 a0001c0001t0001g0233 others(6): Show |
9 | HG00323.hp1 HG01943.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+339delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30988416 | ||||||
| chr17:30988416 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.679+330_679+339del others(10): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30988416 | ||||||
| chr17:30988416 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0081 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.679+327_679+339del others(13): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30988416 | ||||||
| chr17:30988418 | T | G | 1 | a0002c0002t0004g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.679+312T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988418 | |||||||
| chr17:30988466 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.679+360C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988466 | |||||||
| chr17:30988470 | CAGGCTGG others(8): Show |
C | 1 | a0004c0004t0001g0092 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.679+365_679+379del others(15): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988470 | |||||||
| chr17:30988476 | G | A | 3 | a0002c0002t0003g0031 a0002c0002t0003g0064 a0002c0002t0003g0075 |
3 | HG03139.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.679+370G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988476 | |||||||
| chr17:30988478 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.679+372A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988478 | |||||||
| chr17:30988486 | G | T | 1 | a0004c0004t0001g0092 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.679+380G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988486 | |||||||
| chr17:30988628 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0176 |
2 | HG01123.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.679+522A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988628 | |||||||
| chr17:30988716 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.679+610G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988716 | |||||||
| chr17:30988717 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.679+611T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988717 | |||||||
| chr17:30988755 | C | CT | 5 | a0001c0001t0001g0160 a0002c0002t0003g0064 a0002c0002t0004g0244 others(2): Show |
5 | HG01346.hp1 HG01981.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+663dupT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30988755 | ||||||
| chr17:30988758 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.679+652T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30988758 | |||||||
| chr17:30988924 | CT | C | 16 | a0001c0001t0001g0082 a0001c0001t0001g0131 a0001c0001t0001g0132 others(13): Show |
18 | HG01070.hp1 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.679+838delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30988924 | ||||||
| chr17:30988924 | CTT | C | 53 | a0001c0001t0001g0233 a0001c0001t0002g0211 a0002c0002t0001g0004 others(50): Show |
59 | HG00738.hp1 HG01071.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.679+837_679+838del others(2): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30988924 | ||||||
| chr17:30989017 | C | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.679+911C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30989017 | |||||||
| chr17:30989086 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.679+980T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30989086 | |||||||
| chr17:30989517 | T | C | 1 | a0002c0002t0003g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.679+1411T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30989517 | |||||||
| chr17:30989984 | C | CA | 54 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0122 others(51): Show |
59 | HG00738.hp1 HG01071.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.679+1899dupA | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30989984 | ||||||
| chr17:30989984 | C | CAA | 8 | a0001c0001t0001g0192 a0001c0001t0001g0233 a0002c0002t0001g0004 others(5): Show |
9 | HG00438.hp1 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.679+1898_679+1899d others(4): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30989984 | ||||||
| chr17:30990058 | T | A | 49 | a0001c0001t0002g0136 a0001c0001t0002g0211 a0002c0002t0002g0006 others(46): Show |
54 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.679+1952T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990058 | |||||||
| chr17:30990122 | T | C | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+2016T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990122 | |||||||
| chr17:30990249 | G | A | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+2143G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990249 | |||||||
| chr17:30990251 | G | A | 5 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0005c0005t0001g0005 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.679+2145G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990251 | |||||||
| chr17:30990320 | C | CGA | 15 | a0002c0002t0001g0027 a0002c0002t0001g0065 a0002c0002t0003g0024 others(12): Show |
17 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.679+2218_679+2219d others(4): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30990320 | ||||||
| chr17:30990468 | GAGCCACT others(18): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.679+2363_679+2387d others(27): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990468 | |||||||
| chr17:30990587 | G | T | 2 | a0002c0002t0001g0027 a0002c0002t0004g0026 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.679+2481G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990587 | |||||||
| chr17:30990623 | C | G | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.679+2517C>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990623 | |||||||
| chr17:30990669 | C | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.679+2563C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990669 | |||||||
| chr17:30990740 | T | C | 3 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 |
4 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+2634T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990740 | |||||||
| chr17:30990789 | G | T | 4 | a0004c0004t0001g0090 a0004c0004t0001g0091 a0004c0004t0001g0092 others(1): Show |
4 | HG00323.hp1 HG01993.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+2683G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990789 | |||||||
| chr17:30990984 | A | C | 2 | a0002c0002t0002g0060 a0002c0002t0002g0062 |
2 | HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.679+2878A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30990984 | |||||||
| chr17:30991050 | A | G | 2 | a0002c0002t0001g0027 a0002c0002t0004g0026 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.679+2944A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991050 | |||||||
| chr17:30991089 | T | C | 12 | a0002c0002t0002g0006 a0002c0002t0002g0035 a0002c0002t0002g0036 others(9): Show |
13 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.679+2983T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991089 | |||||||
| chr17:30991199 | A | C | 2 | a0002c0002t0003g0024 a0008c0009t0003g0025 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.679+3093A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991199 | |||||||
| chr17:30991253 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.679+3147C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991253 | |||||||
| chr17:30991317 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.679+3211C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991317 | |||||||
| chr17:30991337 | T | A | 5 | a0002c0002t0004g0244 a0002c0002t0004g0245 a0002c0002t0004g0246 others(2): Show |
5 | HG01346.hp1 HG01433.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.679+3231T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991337 | |||||||
| chr17:30991388 | A | G | 1 | a0002c0002t0004g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.679+3282A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991388 | |||||||
| chr17:30991418 | CT | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0123 a0001c0001t0001g0131 others(3): Show |
6 | HG00639.hp1 HG01069.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+3327delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30991418 | ||||||
| chr17:30991480 | G | A | 1 | a0002c0002t0003g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.679+3374G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991480 | |||||||
| chr17:30991593 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.679+3487T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991593 | |||||||
| chr17:30991759 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.679+3653A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991759 | |||||||
| chr17:30991776 | T | C | 41 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0087 others(38): Show |
43 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.679+3670T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30991776 | |||||||
| chr17:30991934 | A | AT | 16 | a0001c0001t0001g0122 a0002c0002t0001g0065 a0002c0002t0003g0024 others(13): Show |
18 | HG01433.hp2 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.679+3843dupT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30991934 | ||||||
| chr17:30991934 | AT | A | 6 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0001g0154 others(3): Show |
6 | HG00323.hp1 HG00408.hp1 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.679+3843delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30991934 | ||||||
| chr17:30992002 | G | A | 5 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0005c0005t0001g0005 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.679+3896G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30992002 | |||||||
| chr17:30992251 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.679+4145A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30992251 | |||||||
| chr17:30992258 | A | T | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.679+4152A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30992258 | |||||||
| chr17:30992371 | A | AT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0082 others(3): Show |
7 | HG02735.hp1 HG02735.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.679+4282dupT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30992371 | ||||||
| chr17:30992505 | T | G | 71 | a0001c0001t0001g0233 a0001c0001t0002g0136 a0001c0001t0002g0211 others(68): Show |
79 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.679+4399T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30992505 | |||||||
| chr17:30992769 | T | A | 48 | a0001c0001t0002g0136 a0001c0001t0002g0211 a0002c0002t0002g0006 others(45): Show |
53 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.680-4473T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30992769 | |||||||
| chr17:30992938 | C | T | 71 | a0001c0001t0001g0233 a0001c0001t0002g0136 a0001c0001t0002g0211 others(68): Show |
79 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.680-4304C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30992938 | |||||||
| chr17:30992998 | A | C | 1 | a0002c0002t0004g0245 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.680-4244A>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30992998 | |||||||
| chr17:30993040 | T | TTTA | 12 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0182 others(9): Show |
12 | HG01346.hp1 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.680-4171_680-4169d others(5): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30993040 | ||||||
| chr17:30993040 | T | TTTATTA | 34 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0002g0136 others(31): Show |
37 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.680-4174_680-4169d others(8): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30993040 | ||||||
| chr17:30993040 | T | TTTATTAT others(2): Show |
19 | a0001c0001t0001g0209 a0001c0001t0001g0233 a0002c0002t0001g0004 others(16): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.680-4177_680-4169d others(11): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30993040 | ||||||
| chr17:30993040 | T | TTTATTAT others(5): Show |
5 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0002g0039 others(2): Show |
5 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.680-4180_680-4169d others(14): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30993040 | ||||||
| chr17:30993040 | T | TTTATTAT others(8): Show |
2 | a0002c0002t0002g0043 a0008c0009t0003g0025 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.680-4183_680-4169d others(17): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30993040 | ||||||
| chr17:30993040 | TTTA | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0138 a0001c0001t0001g0152 others(1): Show |
4 | HG02148.hp2 HG02818.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-4171_680-4169d others(5): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30993040 | ||||||
| chr17:30993147 | G | A | 5 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0005c0005t0001g0005 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-4095G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993147 | |||||||
| chr17:30993305 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.680-3937C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993305 | |||||||
| chr17:30993314 | G | C | 1 | a0002c0006t0003g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.680-3928G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993314 | |||||||
| chr17:30993583 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.680-3659G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993583 | |||||||
| chr17:30993597 | G | A | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.680-3645G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993597 | |||||||
| chr17:30993705 | T | A | 4 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG01167.hp1 HG01192.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-3537T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993705 | |||||||
| chr17:30993757 | A | T | 72 | a0001c0001t0001g0138 a0001c0001t0001g0233 a0001c0001t0002g0136 others(69): Show |
80 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(77): Show |
intron_variant | MODIFIER | c.680-3485A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993757 | |||||||
| chr17:30993820 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.680-3422A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993820 | |||||||
| chr17:30993827 | T | A | 1 | a0002c0002t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.680-3415T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993827 | |||||||
| chr17:30993888 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0211 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.680-3354C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30993888 | |||||||
| chr17:30994063 | C | T | 1 | a0002c0002t0002g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.680-3179C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30994063 | |||||||
| chr17:30994205 | T | C | 4 | a0003c0003t0001g0010 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-3037T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30994205 | |||||||
| chr17:30994244 | T | C | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.680-2998T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30994244 | |||||||
| chr17:30994405 | A | G | 5 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0005c0005t0001g0005 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-2837A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30994405 | |||||||
| chr17:30994502 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.680-2740A>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30994502 | |||||||
| chr17:30994644 | T | A | 4 | a0001c0001t0001g0085 a0001c0001t0001g0099 a0002c0002t0003g0031 others(1): Show |
4 | HG01099.hp2 HG03139.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-2598T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30994644 | |||||||
| chr17:30994712 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.680-2530C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30994712 | |||||||
| chr17:30994736 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.680-2506C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30994736 | |||||||
| chr17:30995029 | A | G | 2 | a0002c0002t0004g0244 a0006c0007t0005g0001 |
4 | HG01346.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-2213A>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30995029 | |||||||
| chr17:30995244 | T | G | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.680-1998T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30995244 | |||||||
| chr17:30995304 | C | T | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.680-1938C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30995304 | |||||||
| chr17:30995531 | T | C | 54 | a0001c0001t0001g0233 a0001c0001t0002g0136 a0001c0001t0002g0211 others(51): Show |
60 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.680-1711T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30995531 | |||||||
| chr17:30995758 | C | CT | 8 | a0001c0001t0001g0182 a0001c0001t0001g0233 a0002c0002t0001g0004 others(5): Show |
9 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.680-1471dupT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30995758 | ||||||
| chr17:30995764 | T | C | 1 | a0002c0002t0002g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.680-1478T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30995764 | |||||||
| chr17:30995777 | G | A | 2 | a0002c0002t0003g0031 a0002c0002t0003g0075 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.680-1465G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30995777 | |||||||
| chr17:30995926 | T | TTG | 12 | a0001c0001t0001g0110 a0001c0001t0001g0175 a0001c0001t0001g0178 others(9): Show |
13 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.680-1294_680-1293d others(4): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30995926 | ||||||
| chr17:30996019 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.680-1223C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30996019 | |||||||
| chr17:30996024 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.680-1218G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30996024 | |||||||
| chr17:30996078 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.680-1164G>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30996078 | |||||||
| chr17:30996088 | CT | C | 47 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0235 others(44): Show |
52 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.680-1134delT | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30996088 | ||||||
| chr17:30996089 | T | C | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.680-1153T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30996089 | |||||||
| chr17:30996161 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.680-1081C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30996161 | |||||||
| chr17:30996395 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.680-847G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30996395 | |||||||
| chr17:30996463 | C | T | 1 | a0002c0002t0004g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.680-779C>T | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30996463 | |||||||
| chr17:30996493 | G | C | 71 | a0001c0001t0001g0233 a0001c0001t0002g0136 a0001c0001t0002g0211 others(68): Show |
79 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.680-749G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30996493 | |||||||
| chr17:30996596 | G | C | 1 | a0002c0002t0004g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.680-646G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30996596 | |||||||
| chr17:30997079 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.680-163T>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30997079 | |||||||
| chr17:30997151 | G | A | 11 | a0002c0002t0003g0024 a0002c0002t0003g0031 a0002c0002t0003g0064 others(8): Show |
11 | HG01346.hp1 HG01433.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.680-91G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30997151 | |||||||
| chr17:30997176 | G | GTCCAAAC others(3): Show |
5 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0005c0005t0001g0005 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-65_680-64insCC others(8): Show |
RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 30997176 | ||||||
| chr17:30997178 | T | C | 5 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0005c0005t0001g0005 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-64T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30997178 | |||||||
| chr17:30997179 | T | C | 5 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0005c0005t0001g0005 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-63T>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30997179 | |||||||
| chr17:30997180 | G | A | 5 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0005c0005t0001g0005 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-62G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30997180 | |||||||
| chr17:30997181 | G | A | 5 | a0002c0006t0001g0226 a0002c0006t0001g0227 a0005c0005t0001g0005 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-61G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 3/4 | chr17 | 30997181 | |||||||
| chr17:30998005 | G | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0079 others(22): Show |
27 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.770-657G>C | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 4/4 | chr17 | 30998005 | |||||||
| chr17:30998520 | G | A | 1 | a0002c0006t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.770-142G>A | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 4/4 | chr17 | 30998520 | |||||||
| chr17:30998606 | T | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0212 |
2 | HG01496.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.770-56T>G | RNF135 | ENSG00000181481.14 | transcript | ENST00000328381.10 | protein_coding | 4/4 | chr17 | 30998606 |