Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1104 |
| ensemblid | ENSG00000180198.17 |
| hgncid | 1913 |
| symbol | RCC1 |
| name | regulator of chromosome condensation 1 |
| refseq_nuc | NM_001381865.2 |
| refseq_prot | NP_001368794.1 |
| ensembl_nuc | ENST00000683442.1 |
| ensembl_prot | ENSP00000508074.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 28506043 |
| end | 28538989 |
| strand | + |
| ver | v1.2 |
| region | chr1:28506043-28538989 |
| region5000 | chr1:28501043-28543989 |
| regionname0 | RCC1_chr1_28506043_28538989 |
| regionname5000 | RCC1_chr1_28501043_28543989 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1263 | 176 | 40 | 39 | 66 | 8 | 21 | RCC1_chr1_28501043_28543989 | RCC1 | ATGTC others(1258): Show |
chr1 | 28501043 | 28543989 | ||
| a0001c0002 | 0/0 | 1263 | 85 | 25 | 23 | 17 | 8 | 12 | RCC1_chr1_28501043_28543989 | RCC1 | ATGTC others(1258): Show |
chr1 | 28501043 | 28543989 | ||
| a0001c0003 | 0/0 | 1263 | 26 | 19 | 4 | 0 | 2 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | ATGTC others(1258): Show |
chr1 | 28501043 | 28543989 | ||
| a0001c0004 | 0/0 | 1263 | 5 | 3 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | ATGTC others(1258): Show |
chr1 | 28501043 | 28543989 | ||
| a0001c0005 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | ATGTC others(1258): Show |
chr1 | 28501043 | 28543989 | ||
| a0001c0006 | 0/0 | 1263 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | ATGTC others(1258): Show |
chr1 | 28501043 | 28543989 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2551 | 155 | 28 | 33 | 66 | 8 | 18 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0001t0002 | 0/0 | 2551 | 5 | 4 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0001t0004 | 0/0 | 2551 | 7 | 6 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0001t0006 | 0/0 | 2518 | 3 | 0 | 2 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2513): Show |
chr1 | 28501043 | 28543989 |
| a0001c0001t0007 | 0/0 | 2549 | 3 | 2 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2544): Show |
chr1 | 28501043 | 28543989 |
| a0001c0001t0008 | 0/0 | 2551 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0001t0009 | 0/0 | 2551 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0001t0011 | 0/0 | 2551 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0002t0001 | 0/0 | 2551 | 63 | 17 | 14 | 16 | 7 | 9 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0002t0002 | 0/0 | 2551 | 6 | 6 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0002t0003 | 0/0 | 2551 | 10 | 1 | 5 | 0 | 1 | 3 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0002t0005 | 0/0 | 2551 | 4 | 0 | 3 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0002t0010 | 0/0 | 2551 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0002t0012 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0003t0001 | 0/0 | 2551 | 2 | 1 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0003t0002 | 0/0 | 2551 | 24 | 18 | 4 | 0 | 1 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0004t0001 | 0/0 | 2551 | 5 | 3 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0005t0002 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| a0001c0006t0001 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | CCTTT others(2546): Show |
chr1 | 28501043 | 28543989 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 7 | 1 | 1 | 3 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0007g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0009g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0001 | 0/0 | 8 | 0 | 4 | 0 | 3 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0005g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0010g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0002t0012g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0004t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0004t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0005t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| a0001c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0065 | EUR | GBR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0011 | EUR | FIN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0240 | EUR | FIN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0069 | EUR | FIN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0022 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0022 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01099 | hp2 | a0001 | c0002 | t0005 | g0056 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01109 | hp1 | a0001 | c0003 | t0002 | g0238 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0044 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0209 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01175 | hp1 | a0001 | c0002 | t0003 | g0208 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01192 | hp2 | a0001 | c0002 | t0010 | g0055 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0082 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0052 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0237 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0239 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0053 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0048 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0176 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0218 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0104 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0253 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01934 | hp1 | a0001 | c0001 | t0009 | g0122 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0210 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0220 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0252 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0054 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02145 | hp2 | a0001 | c0005 | t0002 | g0236 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0226 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0242 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02273 | hp2 | a0001 | c0002 | t0005 | g0058 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02293 | hp2 | a0001 | c0002 | t0005 | g0060 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0040 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0254 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0246 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0228 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02738 | hp2 | a0001 | c0001 | t0008 | g0023 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0249 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0251 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0245 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0248 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0230 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0225 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03130 | hp1 | a0001 | c0003 | t0002 | g0244 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03139 | hp2 | a0001 | c0003 | t0002 | g0219 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0211 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0221 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0214 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0243 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0215 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03669 | hp2 | a0001 | c0001 | t0011 | g0217 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0047 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0250 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0011 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18906 | hp1 | a0001 | c0002 | t0012 | g0224 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0227 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18999 | hp1 | a0001 | c0002 | t0005 | g0057 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0229 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19066 | hp1 | a0001 | c0006 | t0001 | g0167 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0177 | EUR | TSI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | GIH | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0241 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0043 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0213 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0222 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | USA | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0247 | AFR | USA | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0170 | REF | REF | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28507478 | AAAGCTGG others(1184): Show |
A | 1 | a0001 | 3 | HG01167.hp2 HG01978.hp2 HG03239.hp1 |
splice_acceptor_variant&splice_donor_variant&5_prime_UTR_truncation&exon_loss_variant&splice_region_variant&intron_variant | HIGH | c.-261-595_-228-107d others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 28507478 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28532305 | A | C | 1 | a0001c0004 | 5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
synonymous_variant | LOW | c.396A>C | p.Ala132Ala | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/13 | 699/2551 | 396/1266 | 132/421 | chr1 | 28532305 | |||
| chr1:28535124 | G | A | 1 | a0001c0002 | 85 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
synonymous_variant | LOW | c.516G>A | p.Val172Val | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 8/13 | 819/2551 | 516/1266 | 172/421 | chr1 | 28535124 | |||
| chr1:28536766 | C | G | 1 | a0001c0006 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.957C>G | p.Gly319Gly | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/13 | 1260/2551 | 957/1266 | 319/421 | chr1 | 28536766 | |||
| chr1:28536775 | G | A | 1 | a0001c0005 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.966G>A | p.Glu322Glu | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/13 | 1269/2551 | 966/1266 | 322/421 | chr1 | 28536775 | |||
| chr1:28537923 | A | G | 2 | a0001c0003 a0001c0005 |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
synonymous_variant | LOW | c.1182A>G | p.Lys394Lys | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 1485/2551 | 1182/1266 | 394/421 | chr1 | 28537923 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28506070 | C | T | 1 | a0001c0002t0012 | 1 | NA18906.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-276C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/13 | chr1 | 28506070 | |||||||
| chr1:28506074 | T | G | 5 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0012 others(2): Show |
37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-272T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/13 | chr1 | 28506074 | |||||||
| chr1:28506075 | C | T | 1 | a0001c0001t0011 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-271C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/13 | 23792 | chr1 | 28506075 | ||||||
| chr1:28516777 | T | G | 1 | a0001c0001t0004 | 7 | HG00639.hp2 HG02280.hp1 HG03195.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-100T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/13 | 13090 | chr1 | 28516777 | ||||||
| chr1:28516806 | A | G | 1 | a0001c0002t0003 | 10 | HG00280.hp1 HG01123.hp2 HG01167.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-71A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/13 | 13061 | chr1 | 28516806 | ||||||
| chr1:28538104 | C | A | 1 | a0001c0001t0008 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*97C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 97 | chr1 | 28538104 | ||||||
| chr1:28538219 | A | G | 1 | a0001c0002t0005 | 4 | HG01099.hp2 HG02273.hp2 HG02293.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*212A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 212 | chr1 | 28538219 | ||||||
| chr1:28538665 | C | T | 1 | a0001c0002t0010 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*658C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 658 | chr1 | 28538665 | ||||||
| chr1:28538698 | C | T | 1 | a0001c0001t0009 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*691C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 691 | chr1 | 28538698 | ||||||
| chr1:28538756 | GGA | G | 1 | a0001c0001t0007 | 3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*755_*756delAG | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 755 | INFO_REALIGN_3_PRIME | chr1 | 28538756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28506175 | A | G | 37 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(34): Show |
37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-262+91A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506175 | |||||||
| chr1:28506185 | G | A | 37 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(34): Show |
37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-262+101G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506185 | |||||||
| chr1:28506201 | C | CT | 26 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(23): Show |
26 | HG00323.hp1 HG00639.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-262+132dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28506201 | ||||||
| chr1:28506201 | CT | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0008g0023 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-262+132delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28506201 | ||||||
| chr1:28506277 | C | T | 1 | a0001c0004t0001g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-262+193C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506277 | |||||||
| chr1:28506294 | C | T | 4 | a0001c0004t0001g0022 a0001c0004t0001g0213 a0001c0004t0001g0214 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-262+210C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506294 | |||||||
| chr1:28506331 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-262+247C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506331 | |||||||
| chr1:28506411 | C | A | 58 | a0001c0001t0001g0042 a0001c0002t0001g0001 a0001c0002t0001g0004 others(55): Show |
72 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-262+327C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506411 | |||||||
| chr1:28506411 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-262+327C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506411 | |||||||
| chr1:28506519 | C | T | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-262+435C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506519 | |||||||
| chr1:28506558 | A | G | 29 | a0001c0002t0002g0223 a0001c0002t0002g0225 a0001c0002t0002g0226 others(26): Show |
29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-262+474A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506558 | |||||||
| chr1:28506651 | A | G | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-262+567A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506651 | |||||||
| chr1:28506660 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-262+576C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506660 | |||||||
| chr1:28506708 | C | G | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-262+624C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506708 | |||||||
| chr1:28506777 | C | T | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-262+693C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506777 | |||||||
| chr1:28506849 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-262+765G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506849 | |||||||
| chr1:28506919 | C | T | 1 | a0001c0003t0002g0230 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-262+835C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506919 | |||||||
| chr1:28506924 | A | G | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-262+840A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506924 | |||||||
| chr1:28506926 | G | T | 37 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(34): Show |
37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-262+842G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506926 | |||||||
| chr1:28506982 | G | A | 107 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0078 others(104): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.-262+898G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506982 | |||||||
| chr1:28507004 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-262+920C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507004 | |||||||
| chr1:28507024 | CATTTTT | C | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(9): Show |
13 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-262+949_-262+954d others(8): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507024 | ||||||
| chr1:28507131 | G | T | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-261-997G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507131 | |||||||
| chr1:28507137 | T | A | 1 | a0001c0002t0001g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-261-991T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507137 | |||||||
| chr1:28507137 | T | G | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-991T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507137 | |||||||
| chr1:28507213 | G | A | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-915G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507213 | |||||||
| chr1:28507253 | C | T | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-875C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507253 | |||||||
| chr1:28507258 | T | C | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-870T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507258 | |||||||
| chr1:28507296 | T | A | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-832T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507296 | |||||||
| chr1:28507322 | T | A | 35 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(32): Show |
35 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.-261-806T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507322 | |||||||
| chr1:28507339 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-261-789T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507339 | |||||||
| chr1:28507538 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-261-590A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507538 | |||||||
| chr1:28507600 | C | CT | 28 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0018 others(25): Show |
30 | HG00099.hp2 HG00140.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.-261-507dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507600 | ||||||
| chr1:28507600 | CT | C | 68 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0042 others(65): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-261-507delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507600 | ||||||
| chr1:28507600 | CTT | C | 27 | a0001c0001t0001g0137 a0001c0001t0001g0166 a0001c0001t0007g0082 others(24): Show |
28 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-261-508_-261-507d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507600 | ||||||
| chr1:28507600 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0160 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-261-518_-261-507d others(14): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507600 | ||||||
| chr1:28507612 | T | C | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261-516T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507612 | |||||||
| chr1:28507639 | G | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261-489G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507639 | |||||||
| chr1:28507642 | G | T | 58 | a0001c0001t0001g0042 a0001c0002t0001g0001 a0001c0002t0001g0004 others(55): Show |
72 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-261-486G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507642 | |||||||
| chr1:28507816 | A | G | 37 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(34): Show |
37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-261-312A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507816 | |||||||
| chr1:28507886 | G | A | 2 | a0001c0002t0001g0001 a0001c0002t0001g0048 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-261-242G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507886 | |||||||
| chr1:28507907 | G | A | 29 | a0001c0002t0002g0223 a0001c0002t0002g0225 a0001c0002t0002g0226 others(26): Show |
29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-261-221G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507907 | |||||||
| chr1:28507971 | AGCTGGAG others(11): Show |
A | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-261-149_-261-132d others(20): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507971 | ||||||
| chr1:28507978 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0109 others(13): Show |
20 | HG00438.hp2 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.-261-150G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507978 | |||||||
| chr1:28507989 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-261-139C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507989 | |||||||
| chr1:28508074 | G | A | 17 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 others(14): Show |
20 | HG00639.hp1 HG01070.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-261-54G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28508074 | |||||||
| chr1:28508085 | T | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0093 |
3 | HG00280.hp2 HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-261-43T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28508085 | |||||||
| chr1:28508287 | T | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-229+127T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508287 | |||||||
| chr1:28508381 | TAGTC | T | 29 | a0001c0002t0002g0223 a0001c0002t0002g0225 a0001c0002t0002g0226 others(26): Show |
29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-229+224_-229+227d others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 28508381 | ||||||
| chr1:28508529 | G | A | 37 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(34): Show |
37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-228-301G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508529 | |||||||
| chr1:28508587 | T | A | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-228-243T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508587 | |||||||
| chr1:28508660 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-228-170G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508660 | |||||||
| chr1:28508758 | CAT | C | 37 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(34): Show |
37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-228-69_-228-68del others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 28508758 | ||||||
| chr1:28508776 | T | C | 3 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 |
3 | HG01109.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-228-54T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508776 | |||||||
| chr1:28508914 | AT | A | 34 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(31): Show |
34 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-153+20delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28508914 | ||||||
| chr1:28508915 | T | A | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+10T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28508915 | |||||||
| chr1:28508984 | A | C | 1 | a0001c0002t0003g0208 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-153+79A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28508984 | |||||||
| chr1:28509098 | C | T | 13 | a0001c0002t0002g0223 a0001c0002t0002g0225 a0001c0002t0002g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153+193C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509098 | |||||||
| chr1:28509148 | GT | G | 37 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(34): Show |
37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-153+248delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28509148 | ||||||
| chr1:28509298 | C | T | 2 | a0001c0001t0007g0082 a0001c0001t0007g0083 |
2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-153+393C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509298 | |||||||
| chr1:28509371 | AGCTGCGA others(10): Show |
A | 1 | a0001c0003t0002g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-153+468_-153+484d others(19): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28509371 | ||||||
| chr1:28509386 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-153+481C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509386 | |||||||
| chr1:28509466 | C | T | 1 | a0001c0003t0002g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-153+561C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509466 | |||||||
| chr1:28509534 | C | T | 7 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153+629C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509534 | |||||||
| chr1:28509543 | T | C | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+638T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509543 | |||||||
| chr1:28509596 | A | G | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+691A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509596 | |||||||
| chr1:28509902 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-153+997G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509902 | |||||||
| chr1:28510215 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-153+1310A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510215 | |||||||
| chr1:28510277 | T | C | 1 | a0001c0001t0004g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-153+1372T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510277 | |||||||
| chr1:28510288 | G | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
5 | HG01069.hp1 HG02572.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153+1383G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510288 | |||||||
| chr1:28510317 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-153+1412A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510317 | |||||||
| chr1:28510500 | G | A | 49 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(46): Show |
50 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-153+1595G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510500 | |||||||
| chr1:28510585 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-153+1680A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510585 | |||||||
| chr1:28510614 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-153+1709C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510614 | |||||||
| chr1:28510651 | A | G | 1 | a0001c0002t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-153+1746A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510651 | |||||||
| chr1:28510703 | A | T | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+1798A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510703 | |||||||
| chr1:28510895 | A | G | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-153+1990A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510895 | |||||||
| chr1:28510924 | A | T | 109 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0078 others(106): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-153+2019A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510924 | |||||||
| chr1:28510931 | T | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(14): Show |
19 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-153+2026T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510931 | |||||||
| chr1:28511011 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-153+2106C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511011 | |||||||
| chr1:28511063 | T | C | 128 | a0001c0001t0001g0013 a0001c0001t0001g0042 a0001c0001t0001g0077 others(125): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-153+2158T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511063 | |||||||
| chr1:28511077 | A | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0191 a0001c0001t0001g0192 others(2): Show |
7 | HG00558.hp2 HG00738.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153+2172A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511077 | |||||||
| chr1:28511155 | A | G | 8 | a0001c0003t0002g0243 a0001c0003t0002g0244 a0001c0003t0002g0245 others(5): Show |
8 | HG02717.hp2 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-153+2250A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511155 | |||||||
| chr1:28511205 | C | A | 1 | a0001c0003t0002g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-153+2300C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511205 | |||||||
| chr1:28511368 | A | G | 146 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(143): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-153+2463A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511368 | |||||||
| chr1:28511403 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-153+2498G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511403 | |||||||
| chr1:28511403 | GT | G | 48 | a0001c0001t0001g0042 a0001c0001t0007g0083 a0001c0002t0001g0001 others(45): Show |
60 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.-153+2513delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511403 | ||||||
| chr1:28511403 | GTT | G | 44 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(41): Show |
45 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.-153+2512_-153+251 others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511403 | ||||||
| chr1:28511405 | T | G | 5 | a0001c0001t0007g0083 a0001c0002t0002g0254 a0001c0003t0002g0218 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-153+2500T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511405 | |||||||
| chr1:28511406 | T | G | 44 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(41): Show |
45 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.-153+2501T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511406 | |||||||
| chr1:28511408 | T | G | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153+2503T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511408 | |||||||
| chr1:28511429 | C | CT | 49 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(46): Show |
50 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-153+2525dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511429 | ||||||
| chr1:28511432 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-153+2527G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511432 | |||||||
| chr1:28511439 | C | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0088 others(16): Show |
21 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-153+2534C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511439 | |||||||
| chr1:28511521 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-153+2616G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511521 | |||||||
| chr1:28511667 | C | CT | 11 | a0001c0001t0001g0100 a0001c0001t0001g0189 a0001c0002t0001g0075 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-153+2774dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511667 | ||||||
| chr1:28511686 | T | A | 17 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 others(14): Show |
20 | HG00639.hp1 HG01070.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-153+2781T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511686 | |||||||
| chr1:28511686 | T | G | 92 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0078 others(89): Show |
104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-153+2781T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511686 | |||||||
| chr1:28511854 | G | A | 1 | a0001c0003t0002g0230 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-153+2949G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511854 | |||||||
| chr1:28511855 | G | T | 2 | a0001c0001t0001g0188 a0001c0001t0004g0187 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-153+2950G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511855 | |||||||
| chr1:28511962 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-153+3057C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511962 | |||||||
| chr1:28511974 | TC | T | 12 | a0001c0001t0001g0081 a0001c0001t0002g0235 a0001c0002t0002g0252 others(9): Show |
12 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-153+3071delC | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511974 | ||||||
| chr1:28511975 | CCT | C | 37 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(34): Show |
37 | HG00323.hp1 HG01071.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-153+3071_-153+307 others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511975 | |||||||
| chr1:28511976 | C | CT | 7 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(4): Show |
7 | HG01175.hp1 HG01981.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153+3091dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511976 | ||||||
| chr1:28511976 | CT | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(124): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.-153+3091delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511976 | ||||||
| chr1:28512035 | C | T | 8 | a0001c0001t0001g0136 a0001c0002t0001g0070 a0001c0002t0001g0071 others(5): Show |
8 | NA18939.hp2 NA18960.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.-153+3130C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512035 | |||||||
| chr1:28512036 | G | A | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
48 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-153+3131G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512036 | |||||||
| chr1:28512129 | G | A | 9 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0027 others(6): Show |
11 | HG01070.hp2 HG01109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-153+3224G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512129 | |||||||
| chr1:28512178 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-153+3273C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512178 | |||||||
| chr1:28512201 | A | G | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+3296A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512201 | |||||||
| chr1:28512221 | T | TCCACCCG others(37): Show |
109 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0078 others(106): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-153+3321_-153+332 others(48): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28512221 | ||||||
| chr1:28512282 | G | A | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
48 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-153+3377G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512282 | |||||||
| chr1:28512306 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-153+3401C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512306 | |||||||
| chr1:28512419 | ATGTAAAC others(8): Show |
A | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+3516_-153+353 others(19): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28512419 | ||||||
| chr1:28512915 | G | C | 104 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0078 others(101): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-152-3810G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512915 | |||||||
| chr1:28513169 | T | C | 9 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0027 others(6): Show |
11 | HG01070.hp2 HG01109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-152-3556T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513169 | |||||||
| chr1:28513183 | C | T | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-152-3542C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513183 | |||||||
| chr1:28513239 | G | T | 29 | a0001c0002t0002g0223 a0001c0002t0002g0225 a0001c0002t0002g0226 others(26): Show |
29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-152-3486G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513239 | |||||||
| chr1:28513595 | T | A | 1 | a0001c0002t0003g0040 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-152-3130T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513595 | |||||||
| chr1:28513983 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-152-2742A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513983 | |||||||
| chr1:28513989 | C | T | 147 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(144): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-152-2736C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513989 | |||||||
| chr1:28514060 | T | G | 60 | a0001c0001t0001g0042 a0001c0002t0001g0001 a0001c0002t0001g0004 others(57): Show |
74 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.-152-2665T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514060 | |||||||
| chr1:28514156 | C | CA | 6 | a0001c0001t0001g0107 a0001c0001t0001g0137 a0001c0002t0001g0028 others(3): Show |
6 | HG01109.hp2 HG02074.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.-152-2557dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514156 | ||||||
| chr1:28514171 | C | T | 2 | a0001c0002t0001g0059 a0001c0002t0001g0061 |
2 | HG01106.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-152-2554C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514171 | |||||||
| chr1:28514195 | T | A | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-152-2530T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514195 | |||||||
| chr1:28514233 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-152-2492G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514233 | |||||||
| chr1:28514302 | T | G | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-152-2423T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514302 | |||||||
| chr1:28514306 | C | T | 1 | a0001c0001t0004g0105 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-152-2419C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514306 | |||||||
| chr1:28514385 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-152-2340G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514385 | |||||||
| chr1:28514405 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-152-2320G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514405 | |||||||
| chr1:28514428 | C | T | 29 | a0001c0002t0002g0223 a0001c0002t0002g0225 a0001c0002t0002g0226 others(26): Show |
29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-152-2297C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514428 | |||||||
| chr1:28514449 | C | CA | 63 | a0001c0001t0001g0042 a0001c0001t0001g0108 a0001c0001t0001g0189 others(60): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-152-2266dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514449 | ||||||
| chr1:28514449 | CA | C | 29 | a0001c0002t0002g0223 a0001c0002t0002g0225 a0001c0002t0002g0226 others(26): Show |
29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-152-2266delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514449 | ||||||
| chr1:28514460 | C | A | 2 | a0001c0002t0001g0041 a0001c0002t0001g0076 |
2 | HG02300.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-152-2265C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514460 | |||||||
| chr1:28514487 | T | TGTG | 5 | a0001c0001t0004g0016 a0001c0001t0004g0086 a0001c0001t0004g0103 others(2): Show |
6 | HG01884.hp2 HG02280.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-152-2233_-152-223 others(7): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514487 | ||||||
| chr1:28514704 | T | C | 1 | a0001c0003t0002g0244 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-152-2021T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514704 | |||||||
| chr1:28514732 | G | T | 7 | a0001c0002t0001g0070 a0001c0002t0001g0071 a0001c0002t0001g0072 others(4): Show |
7 | NA18939.hp2 NA18960.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-152-1993G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514732 | |||||||
| chr1:28514744 | A | G | 1 | a0001c0002t0001g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-152-1981A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514744 | |||||||
| chr1:28514851 | G | A | 1 | a0001c0005t0002g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-152-1874G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514851 | |||||||
| chr1:28514856 | C | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0178 |
2 | HG02080.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-152-1869C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514856 | |||||||
| chr1:28514862 | G | A | 1 | a0001c0002t0001g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-152-1863G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514862 | |||||||
| chr1:28514870 | G | A | 1 | a0001c0001t0006g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-152-1855G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514870 | |||||||
| chr1:28514878 | AAAAT | A | 5 | a0001c0002t0001g0025 a0001c0003t0002g0218 a0001c0003t0002g0219 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-152-1837_-152-183 others(8): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514878 | ||||||
| chr1:28515005 | C | G | 1 | a0001c0002t0001g0033 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-152-1720C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515005 | |||||||
| chr1:28515114 | CCAAAAAT others(1): Show |
C | 4 | a0001c0004t0001g0022 a0001c0004t0001g0213 a0001c0004t0001g0214 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-152-1603_-152-159 others(12): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28515114 | ||||||
| chr1:28515213 | C | T | 3 | a0001c0002t0005g0056 a0001c0002t0005g0057 a0001c0002t0005g0058 |
3 | HG01099.hp2 HG02273.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-152-1512C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515213 | |||||||
| chr1:28515246 | C | A | 16 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0088 others(13): Show |
18 | HG00639.hp2 HG01069.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.-152-1479C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515246 | |||||||
| chr1:28515521 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-152-1204G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515521 | |||||||
| chr1:28515574 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-152-1151G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515574 | |||||||
| chr1:28515697 | A | G | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-152-1028A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515697 | |||||||
| chr1:28515828 | C | T | 64 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(61): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-152-897C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515828 | |||||||
| chr1:28515876 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-152-849G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515876 | |||||||
| chr1:28516127 | G | A | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-152-598G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28516127 | |||||||
| chr1:28516137 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-152-588C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28516137 | |||||||
| chr1:28516239 | C | T | 1 | a0001c0003t0002g0230 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-152-486C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28516239 | |||||||
| chr1:28516501 | CA | C | 94 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0026 others(91): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-152-207delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28516501 | ||||||
| chr1:28516501 | CAA | C | 32 | a0001c0001t0001g0098 a0001c0002t0001g0028 a0001c0002t0001g0029 others(29): Show |
32 | HG00323.hp1 HG00323.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-152-208_-152-207d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28516501 | ||||||
| chr1:28516678 | CA | C | 6 | a0001c0001t0004g0016 a0001c0001t0004g0086 a0001c0001t0004g0101 others(3): Show |
7 | HG00639.hp2 HG02280.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-152-43delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28516678 | ||||||
| chr1:28517111 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-10+244G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517111 | |||||||
| chr1:28517121 | C | CA | 6 | a0001c0001t0001g0109 a0001c0002t0001g0034 a0001c0002t0002g0223 others(3): Show |
6 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+267dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28517121 | ||||||
| chr1:28517128 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-10+261A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517128 | |||||||
| chr1:28517198 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-10+331A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517198 | |||||||
| chr1:28517249 | T | C | 6 | a0001c0001t0004g0016 a0001c0001t0004g0086 a0001c0001t0004g0101 others(3): Show |
7 | HG00639.hp2 HG02280.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+382T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517249 | |||||||
| chr1:28517369 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-10+502C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517369 | |||||||
| chr1:28517543 | CTTG | C | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+679_-10+681del others(3): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28517543 | ||||||
| chr1:28517584 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-10+717C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517584 | |||||||
| chr1:28517763 | TG | T | 6 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+898delG | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28517763 | ||||||
| chr1:28517807 | C | T | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-10+940C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517807 | |||||||
| chr1:28517981 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | NA19010.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-10+1114C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517981 | |||||||
| chr1:28518080 | C | G | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-10+1213C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518080 | |||||||
| chr1:28518100 | T | TGGCCAAG others(14): Show |
2 | a0001c0002t0003g0043 a0001c0002t0003g0044 |
2 | HG01123.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-10+1257_-10+1277d others(23): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28518100 | ||||||
| chr1:28518100 | TGGCCAAG others(14): Show |
T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
5 | HG01069.hp1 HG02572.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+1257_-10+1277d others(23): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28518100 | ||||||
| chr1:28518111 | TCCCCCAG others(21): Show |
T | 1 | a0001c0001t0004g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-10+1248_-10+1275d others(30): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28518111 | ||||||
| chr1:28518192 | C | T | 4 | a0001c0001t0001g0108 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | NA19054.hp1 NA19078.hp2 NA19089.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+1325C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518192 | |||||||
| chr1:28518259 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-10+1392C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518259 | |||||||
| chr1:28518413 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10+1546C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518413 | |||||||
| chr1:28518499 | GGGGCGCT others(12): Show |
G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+1640_-10+1658d others(21): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28518499 | ||||||
| chr1:28518512 | A | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(245): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-10+1645A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518512 | |||||||
| chr1:28518525 | T | C | 115 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(112): Show |
130 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-10+1658T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518525 | |||||||
| chr1:28518583 | C | G | 1 | a0001c0002t0002g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10+1716C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518583 | |||||||
| chr1:28518723 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-10+1856G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518723 | |||||||
| chr1:28518821 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-10+1954C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518821 | |||||||
| chr1:28518914 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10+2047C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518914 | |||||||
| chr1:28518937 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0139 |
2 | HG00673.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-10+2070C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518937 | |||||||
| chr1:28519204 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-10+2337A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519204 | |||||||
| chr1:28519301 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-10+2434C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519301 | |||||||
| chr1:28519463 | T | C | 1 | a0001c0002t0001g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-10+2596T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519463 | |||||||
| chr1:28519464 | C | T | 94 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(91): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-10+2597C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519464 | |||||||
| chr1:28519551 | G | T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | HG02074.hp1 NA18964.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+2684G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519551 | |||||||
| chr1:28519570 | A | AT | 17 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0079 others(14): Show |
19 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+2716dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28519570 | ||||||
| chr1:28519598 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-10+2731A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519598 | |||||||
| chr1:28519751 | T | C | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-10+2884T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519751 | |||||||
| chr1:28519931 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-10+3064G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519931 | |||||||
| chr1:28520115 | C | G | 5 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0027 others(2): Show |
7 | HG01070.hp2 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+3248C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520115 | |||||||
| chr1:28520128 | A | G | 1 | a0001c0002t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-10+3261A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520128 | |||||||
| chr1:28520382 | G | A | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10+3515G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520382 | |||||||
| chr1:28520400 | G | A | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+3533G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520400 | |||||||
| chr1:28520478 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-10+3611T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520478 | |||||||
| chr1:28520594 | G | A | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+3727G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520594 | |||||||
| chr1:28520637 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-10+3770G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520637 | |||||||
| chr1:28520701 | G | A | 1 | a0001c0002t0001g0045 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-10+3834G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520701 | |||||||
| chr1:28520763 | C | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(10): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+3896C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520763 | |||||||
| chr1:28520800 | G | A | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10+3933G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520800 | |||||||
| chr1:28520989 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-10+4122G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520989 | |||||||
| chr1:28521018 | G | A | 67 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(64): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-10+4151G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521018 | |||||||
| chr1:28521318 | G | C | 1 | a0001c0001t0011g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-10+4451G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521318 | |||||||
| chr1:28521393 | C | G | 1 | a0001c0002t0010g0055 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-10+4526C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521393 | |||||||
| chr1:28521452 | T | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(10): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+4585T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521452 | |||||||
| chr1:28521499 | C | CA | 20 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(17): Show |
20 | HG01109.hp1 HG01243.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+4633dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28521499 | ||||||
| chr1:28521499 | C | CAA | 5 | a0001c0001t0002g0231 a0001c0002t0002g0254 a0001c0004t0001g0022 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+4633_-10+4634i others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28521499 | ||||||
| chr1:28521499 | CAGAAAAA others(4): Show |
C | 68 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(65): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.-10+4634_-10+4644d others(13): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28521499 | ||||||
| chr1:28521501 | G | A | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
48 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10+4634G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521501 | |||||||
| chr1:28521501 | G | GA | 18 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0018 others(15): Show |
19 | HG00673.hp1 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+4656dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28521501 | ||||||
| chr1:28521857 | C | A | 2 | a0001c0002t0001g0007 a0001c0002t0001g0031 |
3 | HG03041.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-10+4990C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521857 | |||||||
| chr1:28522076 | G | T | 67 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(64): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-10+5209G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28522076 | |||||||
| chr1:28522763 | C | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(10): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+5896C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28522763 | |||||||
| chr1:28522804 | A | G | 131 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0078 others(128): Show |
148 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-10+5937A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28522804 | |||||||
| chr1:28523027 | C | CT | 71 | a0001c0001t0001g0021 a0001c0001t0001g0077 a0001c0001t0001g0078 others(68): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-10+6182dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28523027 | ||||||
| chr1:28523027 | C | CTT | 12 | a0001c0001t0001g0162 a0001c0001t0007g0083 a0001c0002t0001g0030 others(9): Show |
12 | HG01175.hp2 HG02080.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10+6181_-10+6182d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28523027 | ||||||
| chr1:28523027 | CT | C | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0132 others(8): Show |
11 | HG01257.hp2 HG01358.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+6182delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28523027 | ||||||
| chr1:28523033 | T | C | 10 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0238 others(7): Show |
10 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+6166T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523033 | |||||||
| chr1:28523034 | T | C | 1 | a0001c0003t0002g0237 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10+6167T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523034 | |||||||
| chr1:28523116 | C | T | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+6249C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523116 | |||||||
| chr1:28523255 | A | T | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10+6388A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523255 | |||||||
| chr1:28523473 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-9-6385G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523473 | |||||||
| chr1:28523615 | G | A | 1 | a0001c0002t0001g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9-6243G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523615 | |||||||
| chr1:28523972 | C | T | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9-5886C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523972 | |||||||
| chr1:28524495 | G | C | 2 | a0001c0001t0004g0101 a0001c0001t0004g0187 |
2 | HG00639.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9-5363G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524495 | |||||||
| chr1:28524533 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-9-5325G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524533 | |||||||
| chr1:28524551 | C | T | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-9-5307C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524551 | |||||||
| chr1:28524617 | G | T | 1 | a0001c0002t0003g0040 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-9-5241G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524617 | |||||||
| chr1:28524626 | G | C | 2 | a0001c0003t0002g0237 a0001c0003t0002g0239 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-9-5232G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524626 | |||||||
| chr1:28524801 | C | T | 1 | a0001c0002t0001g0041 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-9-5057C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524801 | |||||||
| chr1:28525040 | C | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4818C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525040 | |||||||
| chr1:28525103 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-9-4755C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525103 | |||||||
| chr1:28525147 | T | C | 26 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(23): Show |
26 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-9-4711T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525147 | |||||||
| chr1:28525150 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-9-4708A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525150 | |||||||
| chr1:28525261 | C | G | 10 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
11 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-4597C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525261 | |||||||
| chr1:28525588 | G | A | 1 | a0001c0002t0003g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-9-4270G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525588 | |||||||
| chr1:28525680 | A | C | 1 | a0001c0002t0002g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-9-4178A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525680 | |||||||
| chr1:28525726 | T | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4132T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525726 | |||||||
| chr1:28526233 | C | G | 1 | a0001c0002t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-9-3625C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526233 | |||||||
| chr1:28526234 | G | C | 1 | a0001c0002t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-9-3624G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526234 | |||||||
| chr1:28526290 | AAAAC | A | 3 | a0001c0001t0001g0114 a0001c0002t0002g0252 a0001c0002t0002g0253 |
3 | HG01891.hp2 HG02055.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-9-3548_-9-3545del others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28526290 | ||||||
| chr1:28526335 | T | C | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-9-3523T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526335 | |||||||
| chr1:28526393 | C | T | 1 | a0001c0002t0001g0032 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-3465C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526393 | |||||||
| chr1:28526492 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-9-3366G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526492 | |||||||
| chr1:28526757 | G | A | 2 | a0001c0003t0001g0102 a0001c0003t0002g0251 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-9-3101G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526757 | |||||||
| chr1:28526828 | G | C | 114 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(111): Show |
129 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-9-3030G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526828 | |||||||
| chr1:28526864 | T | C | 67 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(64): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-9-2994T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526864 | |||||||
| chr1:28526898 | G | A | 1 | a0001c0002t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-9-2960G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526898 | |||||||
| chr1:28526898 | G | GA | 7 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0001g0116 others(4): Show |
7 | HG00438.hp2 HG02559.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-2945dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28526898 | ||||||
| chr1:28526899 | A | G | 1 | a0001c0002t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-9-2959A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526899 | |||||||
| chr1:28527033 | G | C | 3 | a0001c0001t0002g0232 a0001c0001t0002g0234 a0001c0001t0002g0235 |
3 | HG01255.hp1 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-9-2825G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527033 | |||||||
| chr1:28527069 | G | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0109 a0001c0001t0001g0145 others(1): Show |
9 | HG00438.hp2 HG00558.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-2789G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527069 | |||||||
| chr1:28527186 | G | A | 1 | a0001c0002t0003g0047 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9-2672G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527186 | |||||||
| chr1:28527266 | G | A | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9-2592G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527266 | |||||||
| chr1:28527347 | C | G | 67 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(64): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-9-2511C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527347 | |||||||
| chr1:28527353 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-9-2505C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527353 | |||||||
| chr1:28527401 | G | A | 1 | a0001c0003t0002g0245 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-9-2457G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527401 | |||||||
| chr1:28527712 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-9-2146A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527712 | |||||||
| chr1:28527816 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9-2042C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527816 | |||||||
| chr1:28527866 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-9-1992G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527866 | |||||||
| chr1:28527910 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-9-1948G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527910 | |||||||
| chr1:28528009 | C | CA | 48 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(45): Show |
49 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-9-1830dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528009 | ||||||
| chr1:28528009 | CA | C | 65 | a0001c0001t0001g0132 a0001c0001t0001g0158 a0001c0002t0001g0001 others(62): Show |
78 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.-9-1830delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528009 | ||||||
| chr1:28528119 | G | A | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-9-1739G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528119 | |||||||
| chr1:28528136 | A | G | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-9-1722A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528136 | |||||||
| chr1:28528194 | G | A | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9-1664G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528194 | |||||||
| chr1:28528248 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-9-1610G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528248 | |||||||
| chr1:28528325 | G | A | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1533G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528325 | |||||||
| chr1:28528344 | T | A | 35 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0010 others(32): Show |
45 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.-9-1514T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528344 | |||||||
| chr1:28528391 | G | A | 1 | a0001c0003t0002g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-9-1467G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528391 | |||||||
| chr1:28528450 | A | G | 70 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(67): Show |
84 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-9-1408A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528450 | |||||||
| chr1:28528592 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9-1266C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528592 | |||||||
| chr1:28528691 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-9-1167C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528691 | |||||||
| chr1:28528796 | A | AT | 9 | a0001c0002t0003g0011 a0001c0002t0003g0040 a0001c0002t0003g0043 others(6): Show |
10 | HG00280.hp1 HG01123.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-1054dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528796 | ||||||
| chr1:28528804 | T | TTC | 18 | a0001c0001t0001g0160 a0001c0003t0002g0218 a0001c0003t0002g0219 others(15): Show |
18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9-1054_-9-1053ins others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528804 | |||||||
| chr1:28528805 | C | T | 10 | a0001c0002t0001g0085 a0001c0003t0001g0102 a0001c0003t0001g0176 others(7): Show |
10 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-1053C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528805 | |||||||
| chr1:28528806 | C | A | 18 | a0001c0001t0001g0160 a0001c0003t0002g0218 a0001c0003t0002g0219 others(15): Show |
18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9-1052C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528806 | |||||||
| chr1:28528806 | C | CA | 13 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(10): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-1038dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528806 | ||||||
| chr1:28528806 | C | CAA | 7 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(4): Show |
7 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-1039_-9-1038dup others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528806 | ||||||
| chr1:28528806 | C | CCAA | 9 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0237 others(6): Show |
9 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-1052_-9-1051ins others(3): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528806 | |||||||
| chr1:28528806 | CA | C | 56 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(53): Show |
69 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.-9-1038delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528806 | ||||||
| chr1:28528807 | A | C | 1 | a0001c0002t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-9-1051A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528807 | |||||||
| chr1:28528820 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-9-1038A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528820 | |||||||
| chr1:28528844 | C | CT | 95 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0077 others(92): Show |
111 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(108): Show |
intron_variant | MODIFIER | c.-9-994dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528844 | ||||||
| chr1:28528844 | C | CTT | 11 | a0001c0001t0001g0081 a0001c0001t0001g0133 a0001c0001t0007g0104 others(8): Show |
11 | HG01175.hp1 HG01884.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9-995_-9-994dupTT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528844 | ||||||
| chr1:28528844 | CT | C | 11 | a0001c0003t0001g0176 a0001c0003t0002g0220 a0001c0003t0002g0227 others(8): Show |
11 | HG01516.hp2 HG02055.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-994delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528844 | ||||||
| chr1:28528870 | G | C | 70 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(67): Show |
84 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-9-988G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528870 | |||||||
| chr1:28528940 | G | T | 8 | a0001c0001t0001g0081 a0001c0001t0007g0082 a0001c0001t0007g0083 others(5): Show |
9 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9-918G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528940 | |||||||
| chr1:28528957 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-9-901G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528957 | |||||||
| chr1:28529037 | A | AT | 39 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0080 others(36): Show |
39 | HG00735.hp1 HG01106.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.-9-804dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529037 | ||||||
| chr1:28529037 | AT | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0116 a0001c0001t0001g0125 others(12): Show |
16 | HG01255.hp1 HG02451.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-804delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529037 | ||||||
| chr1:28529039 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0189 |
2 | NA19060.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-9-819T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28529039 | |||||||
| chr1:28529163 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-695G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28529163 | |||||||
| chr1:28529182 | C | CT | 55 | a0001c0001t0001g0005 a0001c0001t0001g0078 a0001c0001t0001g0079 others(52): Show |
59 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.-9-655dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529182 | ||||||
| chr1:28529182 | C | CTT | 60 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0205 others(57): Show |
73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-9-656_-9-655dupTT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529182 | ||||||
| chr1:28529182 | C | CTTT | 14 | a0001c0002t0001g0010 a0001c0002t0001g0038 a0001c0002t0001g0045 others(11): Show |
15 | HG02148.hp1 HG02257.hp2 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-657_-9-655dupTT others(1): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529182 | ||||||
| chr1:28529373 | G | A | 2 | a0001c0003t0001g0102 a0001c0003t0002g0251 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-9-485G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28529373 | |||||||
| chr1:28529697 | CTG | C | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9-158_-9-157delTG | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529697 | ||||||
| chr1:28530157 | C | CA | 12 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0001g0130 others(9): Show |
14 | HG00558.hp2 HG00738.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.73+237dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28530157 | ||||||
| chr1:28530157 | CA | C | 50 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(47): Show |
55 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.73+237delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28530157 | ||||||
| chr1:28530157 | CAA | C | 68 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(65): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.73+236_73+237delAA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28530157 | ||||||
| chr1:28530161 | A | C | 67 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(64): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.73+222A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530161 | |||||||
| chr1:28530163 | A | C | 67 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(64): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.73+224A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530163 | |||||||
| chr1:28530165 | A | C | 67 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(64): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.73+226A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530165 | |||||||
| chr1:28530167 | A | C | 44 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0010 others(41): Show |
55 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.73+228A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530167 | |||||||
| chr1:28530404 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.73+465G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530404 | |||||||
| chr1:28530624 | G | A | 1 | a0001c0002t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.73+685G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530624 | |||||||
| chr1:28530630 | G | A | 1 | a0001c0002t0001g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73+691G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530630 | |||||||
| chr1:28530635 | G | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0152 |
3 | NA18995.hp1 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.73+696G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530635 | |||||||
| chr1:28530786 | C | T | 2 | a0001c0003t0001g0102 a0001c0003t0002g0251 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.73+847C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530786 | |||||||
| chr1:28530824 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.73+885G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530824 | |||||||
| chr1:28530839 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.73+900C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530839 | |||||||
| chr1:28530840 | G | A | 1 | a0001c0003t0002g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.73+901G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530840 | |||||||
| chr1:28530884 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.74-919G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530884 | |||||||
| chr1:28531144 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0175 |
2 | HG00597.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.74-659G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531144 | |||||||
| chr1:28531154 | G | A | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.74-649G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531154 | |||||||
| chr1:28531160 | C | T | 2 | a0001c0003t0001g0102 a0001c0003t0002g0251 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.74-643C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531160 | |||||||
| chr1:28531234 | C | T | 7 | a0001c0003t0001g0176 a0001c0003t0002g0237 a0001c0003t0002g0238 others(4): Show |
7 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-569C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531234 | |||||||
| chr1:28531259 | C | CT | 9 | a0001c0001t0001g0077 a0001c0002t0002g0253 a0001c0003t0002g0220 others(6): Show |
9 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.74-539dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28531259 | ||||||
| chr1:28531259 | C | CTT | 3 | a0001c0002t0001g0048 a0001c0002t0002g0252 a0001c0003t0002g0242 |
3 | HG01516.hp1 HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.74-540_74-539dupTT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28531259 | ||||||
| chr1:28531259 | C | CTTT | 41 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0010 others(38): Show |
52 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.74-541_74-539dupTT others(1): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28531259 | ||||||
| chr1:28531259 | C | CTTTT | 14 | a0001c0002t0001g0009 a0001c0002t0001g0025 a0001c0002t0001g0035 others(11): Show |
15 | HG00741.hp1 HG01106.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.74-542_74-539dupTT others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28531259 | ||||||
| chr1:28531264 | TC | T | 13 | a0001c0001t0001g0081 a0001c0001t0007g0082 a0001c0001t0007g0104 others(10): Show |
14 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.74-538delC | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531264 | |||||||
| chr1:28531265 | C | T | 103 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(100): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.74-538C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531265 | |||||||
| chr1:28531270 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.74-533T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531270 | |||||||
| chr1:28531361 | G | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.74-442G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531361 | |||||||
| chr1:28531457 | C | G | 68 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(65): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.74-346C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531457 | |||||||
| chr1:28531631 | G | A | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.74-172G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531631 | |||||||
| chr1:28531632 | AGAGGTAC others(3): Show |
A | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.74-170_74-161delGA others(8): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531632 | |||||||
| chr1:28532796 | T | TTTG | 3 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG02970.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.441+467_441+469dup others(3): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28532796 | ||||||
| chr1:28532796 | TTTG | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0163 a0001c0001t0001g0206 |
3 | HG02572.hp1 HG02723.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.441+467_441+469del others(3): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28532796 | ||||||
| chr1:28532926 | C | T | 1 | a0001c0003t0002g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.441+576C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28532926 | |||||||
| chr1:28532958 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.441+608G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28532958 | |||||||
| chr1:28533078 | T | A | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG00735.hp1 HG00741.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+728T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533078 | |||||||
| chr1:28533196 | G | T | 1 | a0001c0003t0002g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.441+846G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533196 | |||||||
| chr1:28533197 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG03927.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.441+847C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533197 | |||||||
| chr1:28533254 | G | A | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG00735.hp1 HG00741.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+904G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533254 | |||||||
| chr1:28533276 | A | C | 2 | a0001c0002t0002g0252 a0001c0002t0002g0253 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.441+926A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533276 | |||||||
| chr1:28533399 | A | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+1049A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533399 | |||||||
| chr1:28533427 | C | T | 8 | a0001c0003t0001g0176 a0001c0003t0002g0237 a0001c0003t0002g0238 others(5): Show |
8 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+1077C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533427 | |||||||
| chr1:28533428 | G | A | 2 | a0001c0001t0001g0142 a0001c0002t0001g0216 |
2 | HG00639.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.441+1078G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533428 | |||||||
| chr1:28533447 | G | C | 3 | a0001c0003t0001g0102 a0001c0003t0002g0243 a0001c0003t0002g0251 |
3 | HG02809.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.441+1097G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533447 | |||||||
| chr1:28533702 | G | A | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-1348G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533702 | |||||||
| chr1:28533718 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.442-1332C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533718 | |||||||
| chr1:28533719 | G | A | 1 | a0001c0002t0001g0049 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.442-1331G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533719 | |||||||
| chr1:28533758 | G | A | 1 | a0001c0003t0002g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.442-1292G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533758 | |||||||
| chr1:28533770 | C | CA | 32 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0087 others(29): Show |
34 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.442-1255dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | ||||||
| chr1:28533770 | CA | C | 30 | a0001c0001t0001g0099 a0001c0001t0001g0120 a0001c0001t0001g0138 others(27): Show |
30 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.442-1255delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | ||||||
| chr1:28533770 | CAA | C | 9 | a0001c0002t0001g0039 a0001c0002t0001g0050 a0001c0002t0001g0066 others(6): Show |
9 | HG00639.hp1 HG00741.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-1256_442-1255d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | ||||||
| chr1:28533770 | CAAA | C | 68 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(65): Show |
83 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.442-1257_442-1255d others(5): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | ||||||
| chr1:28533770 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0012g0224 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.442-1264_442-1255d others(12): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | ||||||
| chr1:28533771 | A | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0178 |
2 | HG02080.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.442-1279A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533771 | |||||||
| chr1:28533840 | CTTTTCTT others(24): Show |
C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0193 |
2 | HG03471.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.442-1205_442-1175d others(33): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533840 | ||||||
| chr1:28533840 | CTTTTCTT others(25): Show |
C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02970.hp1 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-1205_442-1174d others(34): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533840 | ||||||
| chr1:28533840 | CTTTTCTT others(26): Show |
C | 4 | a0001c0004t0001g0022 a0001c0004t0001g0213 a0001c0004t0001g0214 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-1205_442-1173d others(35): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533840 | ||||||
| chr1:28533840 | CTTTTCTT others(27): Show |
C | 4 | a0001c0001t0001g0081 a0001c0001t0007g0082 a0001c0001t0007g0083 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1205_442-1172d others(36): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533840 | ||||||
| chr1:28533845 | C | CT | 8 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0098 others(5): Show |
8 | HG00140.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-1155dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | C | CTT | 7 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0097 others(4): Show |
7 | HG02280.hp2 HG02559.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1156_442-1155d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | C | CTTTT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0138 others(3): Show |
7 | HG00438.hp1 HG00735.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1158_442-1155d others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.442-1165_442-1155d others(13): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0133 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.442-1167_442-1155d others(15): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.442-1205C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533845 | |||||||
| chr1:28533845 | CT | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0107 others(13): Show |
16 | HG00738.hp2 HG01167.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1155delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTT | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0096 others(7): Show |
10 | HG00099.hp1 HG00099.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-1156_442-1155d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTT | C | 12 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0135 others(9): Show |
12 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-1157_442-1155d others(5): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTT | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0089 others(5): Show |
8 | HG00558.hp2 HG00639.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-1158_442-1155d others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTT | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
6 | HG02572.hp1 HG02572.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1159_442-1155d others(7): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0200 |
2 | HG04199.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.442-1164_442-1155d others(12): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0181 |
2 | HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.442-1165_442-1155d others(13): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0151 |
2 | HG01081.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.442-1167_442-1155d others(15): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0024 |
3 | HG01258.hp1 HG03491.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.442-1168_442-1155d others(16): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0130 others(2): Show |
5 | HG00673.hp1 HG01081.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1169_442-1155d others(17): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(1): Show |
4 | HG03491.hp2 NA18959.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1170_442-1155d others(18): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0109 a0001c0001t0001g0145 |
3 | HG00438.hp2 HG02165.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.442-1171_442-1155d others(19): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0188 |
5 | HG00558.hp1 HG02155.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1172_442-1155d others(20): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0114 |
2 | NA18612.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.442-1173_442-1155d others(21): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(13): Show |
C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0123 a0001c0001t0001g0158 others(4): Show |
7 | HG03831.hp2 NA18939.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-1174_442-1155d others(22): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(15): Show |
C | 6 | a0001c0003t0002g0220 a0001c0003t0002g0222 a0001c0003t0002g0227 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1176_442-1155d others(24): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(16): Show |
C | 8 | a0001c0003t0002g0221 a0001c0003t0002g0228 a0001c0003t0002g0230 others(5): Show |
8 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-1177_442-1155d others(25): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(17): Show |
C | 14 | a0001c0001t0001g0106 a0001c0003t0001g0102 a0001c0003t0001g0176 others(11): Show |
14 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-1178_442-1155d others(26): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(18): Show |
C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0100 a0001c0001t0001g0199 |
3 | HG04204.hp1 NA18947.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.442-1179_442-1155d others(27): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(19): Show |
C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0115 |
2 | HG01106.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.442-1180_442-1155d others(28): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(20): Show |
C | 2 | a0001c0001t0001g0178 a0001c0002t0002g0254 |
2 | HG02080.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.442-1181_442-1155d others(29): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(21): Show |
C | 3 | a0001c0001t0001g0127 a0001c0001t0004g0016 a0001c0001t0004g0086 |
3 | HG02280.hp1 HG02300.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.442-1182_442-1155d others(30): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(25): Show |
C | 7 | a0001c0001t0004g0105 a0001c0002t0001g0010 a0001c0002t0001g0028 others(4): Show |
7 | HG01109.hp2 HG02717.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1186_442-1155d others(34): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(26): Show |
C | 67 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(64): Show |
80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.442-1187_442-1155d others(35): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533845 | CTTTTTTT others(27): Show |
C | 1 | a0001c0002t0001g0049 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.442-1188_442-1155d others(36): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | ||||||
| chr1:28533850 | T | C | 1 | a0001c0002t0002g0252 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.442-1200T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533850 | |||||||
| chr1:28533874 | T | C | 1 | a0001c0003t0002g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.442-1176T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533874 | |||||||
| chr1:28533900 | CAG | C | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-1147_442-1146d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533900 | ||||||
| chr1:28534066 | C | T | 1 | a0001c0002t0001g0216 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.442-984C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534066 | |||||||
| chr1:28534201 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.442-849G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534201 | |||||||
| chr1:28534243 | C | T | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-807C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534243 | |||||||
| chr1:28534295 | C | G | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-755C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534295 | |||||||
| chr1:28534342 | G | A | 45 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(42): Show |
46 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-708G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534342 | |||||||
| chr1:28534422 | C | T | 32 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0078 others(29): Show |
35 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.442-628C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534422 | |||||||
| chr1:28534475 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.442-575C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534475 | |||||||
| chr1:28535004 | G | A | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-46G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28535004 | |||||||
| chr1:28535681 | G | A | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.662-190G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 9/12 | chr1 | 28535681 | |||||||
| chr1:28536089 | A | G | 5 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+63A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 10/12 | chr1 | 28536089 | |||||||
| chr1:28536248 | G | A | 1 | a0001c0002t0001g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.818-14G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 10/12 | chr1 | 28536248 | |||||||
| chr1:28536563 | A | G | 70 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(67): Show |
84 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.937+182A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 11/12 | chr1 | 28536563 | |||||||
| chr1:28536997 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1090+98C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28536997 | |||||||
| chr1:28537024 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
7 | HG01261.hp2 HG01433.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1090+125G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537024 | |||||||
| chr1:28537136 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1090+237G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537136 | |||||||
| chr1:28537305 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1090+406T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537305 | |||||||
| chr1:28537318 | A | G | 14 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(11): Show |
15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1090+419A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537318 | |||||||
| chr1:28537535 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1091-297A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537535 | |||||||
| chr1:28537608 | G | A | 68 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0007 others(65): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1091-224G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537608 | |||||||
| chr1:28537651 | T | A | 27 | a0001c0003t0001g0102 a0001c0003t0001g0176 a0001c0003t0002g0218 others(24): Show |
27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1091-181T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537651 |