Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84816 |
| ensemblid | ENSG00000130347.13 |
| hgncid | 18647 |
| symbol | RTN4IP1 |
| name | reticulon 4 interacting protein 1 |
| refseq_nuc | NM_032730.5 |
| refseq_prot | NP_116119.2 |
| ensembl_nuc | ENST00000369063.8 |
| ensembl_prot | ENSP00000358059.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 106570771 |
| end | 106629498 |
| strand | - |
| ver | v1.2 |
| region | chr6:106570771-106629498 |
| region5000 | chr6:106565771-106634498 |
| regionname0 | RTN4IP1_chr6_106570771_106629498 |
| regionname5000 | RTN4IP1_chr6_106565771_106634498 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 396 | 391 | 90 | 70 | 181 | 14 | 34 | 141 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | MEFLK others(391): Show |
chr6 | 106565771 | 106634498 |
| a0002 | 0/0 | 396 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | MEFLK others(391): Show |
chr6 | 106565771 | 106634498 |
| a0003 | 0/0 | 396 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | MAFLK others(391): Show |
chr6 | 106565771 | 106634498 |
| a0004 | 0/0 | 396 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | MEFLK others(391): Show |
chr6 | 106565771 | 106634498 |
| a0005 | 0/0 | 396 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | MEFLK others(391): Show |
chr6 | 106565771 | 106634498 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1188 | 182 | 27 | 37 | 76 | 11 | 29 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0001c0002 | 0/0 | 1188 | 78 | 12 | 19 | 43 | 2 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0001c0003 | 0/0 | 1188 | 67 | 30 | 6 | 27 | 1 | 3 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0001c0004 | 0/0 | 1188 | 56 | 14 | 8 | 34 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0001c0005 | 0/0 | 1188 | 5 | 5 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0001c0008 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0001c0009 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0001c0011 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0002c0006 | 0/0 | 1188 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0003c0012 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGC others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0004c0007 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 | ||
| a0005c0010 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | ATGGA others(1183): Show |
chr6 | 106565771 | 106634498 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2893 | 164 | 23 | 29 | 73 | 11 | 26 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0001t0005 | 0/0 | 2893 | 9 | 1 | 5 | 0 | 0 | 3 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0001t0007 | 0/0 | 2893 | 5 | 0 | 3 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0001t0010 | 0/0 | 2893 | 3 | 3 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0001t0014 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0002t0001 | 0/0 | 2893 | 36 | 11 | 9 | 12 | 2 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0002t0004 | 0/0 | 2894 | 38 | 0 | 7 | 31 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2889): Show |
chr6 | 106565771 | 106634498 |
| a0001c0002t0009 | 0/0 | 2890 | 4 | 1 | 3 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2885): Show |
chr6 | 106565771 | 106634498 |
| a0001c0003t0002 | 0/0 | 2893 | 55 | 20 | 6 | 25 | 1 | 3 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0003t0006 | 0/0 | 2893 | 8 | 8 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0003t0011 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2889): Show |
chr6 | 106565771 | 106634498 |
| a0001c0003t0012 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0003t0013 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0004t0003 | 0/0 | 2891 | 56 | 14 | 8 | 34 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2886): Show |
chr6 | 106565771 | 106634498 |
| a0001c0005t0008 | 0/0 | 2891 | 5 | 5 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2886): Show |
chr6 | 106565771 | 106634498 |
| a0001c0008t0001 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0009t0006 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0001c0011t0002 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0002c0006t0005 | 0/0 | 2893 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0003c0012t0001 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0004c0007t0001 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| a0005c0010t0002 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | GCAAA others(2888): Show |
chr6 | 106565771 | 106634498 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0005g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0005g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0005g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0005g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0005g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0005g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0005g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0005g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0010g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0014g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0009g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0009g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0009g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0009g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0011g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0011g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0008g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0008g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0008t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0009t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0011t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0002c0006t0005g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0002c0006t0005g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0003c0012t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0004c0007t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0005c0010t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | GBR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0091 | EUR | FIN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | FIN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00408 | hp1 | a0001 | c0002 | t0004 | g0289 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0301 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00423 | hp2 | a0001 | c0004 | t0003 | g0321 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0153 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00544 | hp2 | a0001 | c0004 | t0003 | g0326 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00558 | hp1 | a0001 | c0002 | t0004 | g0285 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0304 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00609 | hp1 | a0001 | c0002 | t0004 | g0295 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00609 | hp2 | a0001 | c0004 | t0003 | g0317 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0094 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0367 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00733 | hp1 | a0001 | c0002 | t0009 | g0306 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0363 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0364 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0268 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0361 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0096 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0154 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0155 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01175 | hp1 | a0001 | c0004 | t0003 | g0314 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0358 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01192 | hp1 | a0001 | c0004 | t0003 | g0352 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0095 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01243 | hp1 | a0001 | c0002 | t0009 | g0307 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0093 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01255 | hp2 | a0001 | c0004 | t0003 | g0353 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01257 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01258 | hp2 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01358 | hp1 | a0001 | c0002 | t0004 | g0001 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0061 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01496 | hp2 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | IBS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0042 | EUR | IBS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | IBS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01884 | hp1 | a0001 | c0004 | t0003 | g0316 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0082 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0105 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01891 | hp2 | a0001 | c0005 | t0008 | g0342 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01928 | hp2 | a0001 | c0002 | t0004 | g0276 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01943 | hp1 | a0001 | c0002 | t0004 | g0293 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01952 | hp1 | a0001 | c0002 | t0004 | g0279 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01952 | hp2 | a0001 | c0002 | t0009 | g0305 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01981 | hp2 | a0001 | c0004 | t0003 | g0351 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01993 | hp2 | a0001 | c0002 | t0004 | g0001 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02004 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0001 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0114 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02027 | hp2 | a0001 | c0004 | t0003 | g0322 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0100 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02055 | hp2 | a0001 | c0004 | t0003 | g0320 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02056 | hp1 | a0001 | c0004 | t0003 | g0340 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02074 | hp1 | a0001 | c0002 | t0004 | g0298 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02074 | hp2 | a0001 | c0003 | t0002 | g0055 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02083 | hp2 | a0001 | c0004 | t0003 | g0338 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02132 | hp1 | a0001 | c0002 | t0004 | g0278 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02132 | hp2 | a0001 | c0004 | t0003 | g0005 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0059 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02145 | hp1 | a0001 | c0004 | t0003 | g0350 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02148 | hp2 | a0001 | c0003 | t0002 | g0046 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CDX | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02257 | hp1 | a0001 | c0003 | t0006 | g0029 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0359 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02273 | hp1 | a0001 | c0002 | t0004 | g0288 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0087 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02280 | hp2 | a0001 | c0004 | t0003 | g0356 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0056 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0104 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02615 | hp1 | a0001 | c0004 | t0003 | g0347 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02615 | hp2 | a0001 | c0005 | t0008 | g0310 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02622 | hp1 | a0001 | c0004 | t0003 | g0343 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02630 | hp1 | a0001 | c0004 | t0003 | g0344 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02647 | hp1 | a0001 | c0003 | t0006 | g0025 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0036 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0360 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02717 | hp2 | a0001 | c0005 | t0008 | g0355 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02723 | hp1 | a0001 | c0004 | t0003 | g0346 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0103 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0083 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02818 | hp1 | a0001 | c0003 | t0006 | g0026 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0052 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0054 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02897 | hp1 | a0001 | c0003 | t0002 | g0053 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02897 | hp2 | a0001 | c0003 | t0006 | g0024 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0116 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02965 | hp1 | a0001 | c0005 | t0008 | g0318 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02965 | hp2 | a0001 | c0004 | t0003 | g0345 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0106 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0032 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03098 | hp1 | a0001 | c0003 | t0006 | g0023 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0086 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0013 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03139 | hp2 | a0001 | c0004 | t0003 | g0312 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0014 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03209 | hp2 | a0003 | c0012 | t0001 | g0275 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03225 | hp2 | a0001 | c0003 | t0006 | g0028 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03453 | hp2 | a0001 | c0003 | t0006 | g0030 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03486 | hp1 | a0001 | c0004 | t0003 | g0309 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03486 | hp2 | a0001 | c0005 | t0008 | g0311 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03491 | hp2 | a0002 | c0006 | t0005 | g0365 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03492 | hp1 | a0002 | c0006 | t0005 | g0366 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0101 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03540 | hp1 | a0001 | c0009 | t0006 | g0031 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03579 | hp2 | a0001 | c0004 | t0003 | g0348 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0362 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0033 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0368 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0037 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0085 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18612 | hp1 | a0001 | c0004 | t0003 | g0354 | EAS | CHB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | CHB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0102 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18906 | hp2 | a0001 | c0003 | t0006 | g0027 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18942 | hp1 | a0001 | c0003 | t0011 | g0303 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18942 | hp2 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18945 | hp1 | a0001 | c0003 | t0002 | g0090 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18945 | hp2 | a0001 | c0004 | t0003 | g0006 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18946 | hp1 | a0001 | c0002 | t0004 | g0281 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18946 | hp2 | a0001 | c0004 | t0003 | g0331 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18947 | hp1 | a0001 | c0004 | t0003 | g0334 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18950 | hp2 | a0001 | c0003 | t0002 | g0049 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0016 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0302 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18959 | hp1 | a0001 | c0004 | t0003 | g0328 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18960 | hp1 | a0001 | c0004 | t0003 | g0335 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18961 | hp1 | a0001 | c0004 | t0003 | g0341 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0286 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18965 | hp2 | a0001 | c0004 | t0003 | g0327 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0294 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18968 | hp1 | a0001 | c0004 | t0003 | g0337 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0291 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18972 | hp2 | a0001 | c0003 | t0002 | g0058 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18973 | hp1 | a0001 | c0004 | t0003 | g0336 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18974 | hp1 | a0005 | c0010 | t0002 | g0110 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18975 | hp2 | a0001 | c0004 | t0003 | g0315 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18978 | hp1 | a0001 | c0004 | t0003 | g0325 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18979 | hp1 | a0001 | c0003 | t0002 | g0009 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18979 | hp2 | a0001 | c0002 | t0004 | g0292 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18982 | hp1 | a0001 | c0004 | t0003 | g0319 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18983 | hp2 | a0001 | c0002 | t0004 | g0016 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18985 | hp1 | a0001 | c0003 | t0002 | g0089 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18989 | hp1 | a0001 | c0002 | t0004 | g0296 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18993 | hp1 | a0001 | c0004 | t0003 | g0005 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18994 | hp1 | a0001 | c0004 | t0003 | g0324 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18995 | hp1 | a0001 | c0003 | t0002 | g0034 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18998 | hp2 | a0001 | c0002 | t0004 | g0287 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18999 | hp1 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19002 | hp2 | a0001 | c0004 | t0003 | g0333 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19004 | hp1 | a0001 | c0003 | t0002 | g0097 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19005 | hp1 | a0001 | c0004 | t0003 | g0006 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19005 | hp2 | a0001 | c0003 | t0002 | g0045 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19010 | hp1 | a0001 | c0004 | t0003 | g0329 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19010 | hp2 | a0001 | c0003 | t0002 | g0012 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19012 | hp1 | a0001 | c0003 | t0002 | g0092 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19012 | hp2 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19030 | hp1 | a0001 | c0004 | t0003 | g0313 | AFR | LWK | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19030 | hp2 | a0001 | c0003 | t0012 | g0020 | AFR | LWK | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19054 | hp1 | a0001 | c0002 | t0004 | g0282 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19055 | hp1 | a0001 | c0002 | t0004 | g0277 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19055 | hp2 | a0001 | c0004 | t0003 | g0006 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19057 | hp1 | a0001 | c0004 | t0003 | g0330 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19057 | hp2 | a0001 | c0002 | t0004 | g0284 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19058 | hp1 | a0001 | c0004 | t0003 | g0339 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19058 | hp2 | a0001 | c0003 | t0002 | g0035 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19064 | hp1 | a0001 | c0003 | t0002 | g0009 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19065 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19066 | hp1 | a0001 | c0003 | t0002 | g0060 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19067 | hp1 | a0001 | c0011 | t0002 | g0112 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19067 | hp2 | a0001 | c0002 | t0004 | g0300 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0290 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19068 | hp2 | a0001 | c0004 | t0003 | g0357 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19070 | hp1 | a0001 | c0003 | t0011 | g0299 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19072 | hp1 | a0001 | c0003 | t0002 | g0022 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19072 | hp2 | a0001 | c0004 | t0003 | g0005 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19076 | hp2 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19078 | hp2 | a0001 | c0003 | t0002 | g0088 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0297 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19081 | hp1 | a0001 | c0003 | t0002 | g0012 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19081 | hp2 | a0001 | c0001 | t0014 | g0245 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19082 | hp1 | a0001 | c0003 | t0002 | g0038 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19084 | hp1 | a0001 | c0004 | t0003 | g0332 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19084 | hp2 | a0001 | c0002 | t0004 | g0280 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19088 | hp1 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19089 | hp2 | a0001 | c0003 | t0002 | g0098 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0283 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0084 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | TSI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | TSI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0014 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | USA | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG06807 | hp2 | a0004 | c0007 | t0001 | g0081 | AFR | USA | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18955 | hp1 | a0001 | c0004 | t0003 | g0323 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20300 | hp1 | a0001 | c0003 | t0013 | g0109 | AFR | USA | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20300 | hp2 | a0001 | c0004 | t0003 | g0349 | AFR | USA | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA21309 | hp1 | a0001 | c0002 | t0009 | g0308 | AFR | LWK | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0256 | REF | REF | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0166 | REF | REF | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106572028 | C | T | 1 | a0002 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.1159G>A | p.Ala387Thr | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1636/2893 | 1159/1191 | 387/396 | chr6 | 106572028 | |||
| chr6:106572093 | A | G | 1 | a0004 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1094T>C | p.Val365Ala | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1571/2893 | 1094/1191 | 365/396 | chr6 | 106572093 | |||
| chr6:106628871 | A | T | 1 | a0005 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.151T>A | p.Tyr51Asn | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 628/2893 | 151/1191 | 51/396 | chr6 | 106628871 | |||
| chr6:106628872 | T | A | 1 | a0005 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.150A>T | p.Lys50Asn | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 627/2893 | 150/1191 | 50/396 | chr6 | 106628872 | |||
| chr6:106629017 | T | G | 1 | a0003 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.5A>C | p.Glu2Ala | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 482/2893 | 5/1191 | 2/396 | chr6 | 106629017 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106572005 | A | G | 5 | a0001c0003 a0001c0005 a0001c0009 others(2): Show |
75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
synonymous_variant | LOW | c.1182T>C | p.Asn394Asn | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1659/2893 | 1182/1191 | 394/396 | chr6 | 106572005 | |||
| chr6:106602898 | G | A | 1 | a0001c0008 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.645C>T | p.Gly215Gly | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/9 | 1122/2893 | 645/1191 | 215/396 | chr6 | 106602898 | |||
| chr6:106619285 | G | A | 1 | a0001c0009 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.537C>T | p.Ala179Ala | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/9 | 1014/2893 | 537/1191 | 179/396 | chr6 | 106619285 | |||
| chr6:106628821 | G | A | 2 | a0001c0004 a0001c0005 |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
synonymous_variant | LOW | c.201C>T | p.Ile67Ile | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 678/2893 | 201/1191 | 67/396 | chr6 | 106628821 | |||
| chr6:106628908 | A | T | 9 | a0001c0002 a0001c0003 a0001c0004 others(6): Show |
211 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(208): Show |
synonymous_variant | LOW | c.114T>A | p.Pro38Pro | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 591/2893 | 114/1191 | 38/396 | chr6 | 106628908 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106570792 | C | T | 3 | a0001c0003t0006 a0001c0003t0013 a0001c0009t0006 |
10 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1204G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1204 | chr6 | 106570792 | ||||||
| chr6:106570799 | A | G | 9 | a0001c0003t0002 a0001c0003t0006 a0001c0003t0011 others(6): Show |
75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1197T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1197 | chr6 | 106570799 | ||||||
| chr6:106570934 | T | G | 1 | a0001c0001t0014 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1062A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1062 | chr6 | 106570934 | ||||||
| chr6:106570964 | G | A | 1 | a0001c0001t0010 | 3 | HG02109.hp1 HG02922.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1032C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1032 | chr6 | 106570964 | ||||||
| chr6:106571079 | T | A | 2 | a0001c0003t0006 a0001c0009t0006 |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*917A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 917 | chr6 | 106571079 | ||||||
| chr6:106571287 | A | G | 1 | a0001c0002t0009 | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*709T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 709 | chr6 | 106571287 | ||||||
| chr6:106571412 | C | T | 9 | a0001c0003t0002 a0001c0003t0006 a0001c0003t0011 others(6): Show |
75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*584G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 584 | chr6 | 106571412 | ||||||
| chr6:106571413 | G | T | 3 | a0001c0001t0005 a0001c0001t0007 a0002c0006t0005 |
16 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*583C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 583 | chr6 | 106571413 | ||||||
| chr6:106571760 | A | G | 6 | a0001c0003t0002 a0001c0003t0011 a0001c0003t0012 others(3): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*236T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 236 | chr6 | 106571760 | ||||||
| chr6:106571785 | C | T | 1 | a0001c0001t0014 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 211 | chr6 | 106571785 | ||||||
| chr6:106571786 | T | C | 9 | a0001c0003t0002 a0001c0003t0006 a0001c0003t0011 others(6): Show |
75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*210A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 210 | chr6 | 106571786 | ||||||
| chr6:106571791 | A | G | 9 | a0001c0003t0002 a0001c0003t0006 a0001c0003t0011 others(6): Show |
75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*205T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 205 | chr6 | 106571791 | ||||||
| chr6:106629184 | G | GA | 2 | a0001c0002t0004 a0001c0003t0011 |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-164dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 164 | chr6 | 106629184 | ||||||
| chr6:106629185 | AAAG | A | 1 | a0001c0002t0009 | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-167_-165delCTT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 165 | chr6 | 106629185 | ||||||
| chr6:106629290 | A | G | 1 | a0001c0003t0012 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-269T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 269 | chr6 | 106629290 | ||||||
| chr6:106629303 | AAG | A | 2 | a0001c0004t0003 a0001c0005t0008 |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-284_-283delCT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 283 | chr6 | 106629303 | ||||||
| chr6:106629305 | G | A | 12 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0004 others(9): Show |
243 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(240): Show |
5_prime_UTR_variant | MODIFIER | c.-284C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 284 | chr6 | 106629305 | ||||||
| chr6:106629435 | G | A | 2 | a0001c0001t0005 a0002c0006t0005 |
11 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-414C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 414 | chr6 | 106629435 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106572119 | G | T | 72 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(69): Show |
75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
intron_variant | MODIFIER | c.1084-16C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572119 | |||||||
| chr6:106572213 | A | G | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-110T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572213 | |||||||
| chr6:106572217 | G | A | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-114C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572217 | |||||||
| chr6:106572314 | C | T | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(272): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1084-211G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572314 | |||||||
| chr6:106572332 | TCTC | T | 29 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0021 others(26): Show |
31 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.1084-232_1084-230d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572332 | |||||||
| chr6:106572400 | G | GA | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-298dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572400 | |||||||
| chr6:106572464 | C | T | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-361G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572464 | |||||||
| chr6:106572525 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1084-422G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572525 | |||||||
| chr6:106572531 | T | C | 1 | a0001c0004t0003g0351 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1084-428A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572531 | |||||||
| chr6:106572574 | T | A | 74 | a0001c0002t0001g0008 a0001c0002t0001g0108 a0001c0003t0002g0009 others(71): Show |
78 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.1084-471A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572574 | |||||||
| chr6:106572596 | G | A | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-493C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572596 | |||||||
| chr6:106572630 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1084-527C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572630 | |||||||
| chr6:106572730 | T | G | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-627A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572730 | |||||||
| chr6:106572741 | T | C | 339 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(336): Show |
365 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.1084-638A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572741 | |||||||
| chr6:106572778 | TTTTGTTT others(4): Show |
T | 1 | a0001c0003t0012g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1084-686_1084-676d others(13): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572778 | |||||||
| chr6:106572779 | TTTGTTTT others(3): Show |
T | 59 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(56): Show |
62 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.1084-686_1084-677d others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572779 | |||||||
| chr6:106572836 | C | A | 2 | a0001c0002t0001g0008 a0001c0002t0001g0108 |
3 | HG02257.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1084-733G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572836 | |||||||
| chr6:106573030 | G | T | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-927C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573030 | |||||||
| chr6:106573153 | C | T | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-1050G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573153 | |||||||
| chr6:106573331 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0224 |
2 | NA18998.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1084-1228T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573331 | |||||||
| chr6:106573609 | G | C | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1084-1506C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573609 | |||||||
| chr6:106573745 | A | G | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-1642T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573745 | |||||||
| chr6:106573756 | C | A | 1 | a0001c0004t0003g0349 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1084-1653G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573756 | |||||||
| chr6:106573768 | G | A | 11 | a0001c0002t0001g0108 a0001c0003t0006g0023 a0001c0003t0006g0024 others(8): Show |
11 | HG02257.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1084-1665C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573768 | |||||||
| chr6:106573928 | C | G | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-1825G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573928 | |||||||
| chr6:106573930 | A | C | 2 | a0001c0002t0001g0008 a0003c0012t0001g0275 |
3 | HG03209.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1084-1827T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573930 | |||||||
| chr6:106573933 | C | T | 31 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(28): Show |
38 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1084-1830G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573933 | |||||||
| chr6:106574082 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0196 |
2 | HG00408.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1084-1979T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574082 | |||||||
| chr6:106574147 | T | C | 1 | a0001c0002t0009g0306 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1084-2044A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574147 | |||||||
| chr6:106574153 | G | A | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2050C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574153 | |||||||
| chr6:106574154 | A | C | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(1): Show |
4 | HG03130.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-2051T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574154 | |||||||
| chr6:106574170 | T | C | 363 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(360): Show |
390 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.1084-2067A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574170 | |||||||
| chr6:106574246 | A | AC | 346 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(343): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1084-2144dupG | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574246 | |||||||
| chr6:106574271 | T | C | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2168A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574271 | |||||||
| chr6:106574317 | T | C | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2214A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574317 | |||||||
| chr6:106574366 | C | T | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2263G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574366 | |||||||
| chr6:106574443 | C | CA | 10 | a0001c0001t0001g0123 a0001c0001t0001g0228 a0001c0001t0001g0244 others(7): Show |
10 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-2341dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574443 | |||||||
| chr6:106574443 | CA | C | 73 | a0001c0002t0001g0008 a0001c0002t0001g0108 a0001c0003t0002g0009 others(70): Show |
77 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.1084-2341delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574443 | |||||||
| chr6:106574520 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(233): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1084-2417A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574520 | |||||||
| chr6:106574585 | T | C | 34 | a0001c0001t0001g0208 a0001c0002t0001g0007 a0001c0002t0001g0010 others(31): Show |
37 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1084-2482A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574585 | |||||||
| chr6:106574590 | G | T | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2487C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574590 | |||||||
| chr6:106574611 | C | T | 1 | a0001c0001t0005g0358 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1084-2508G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574611 | |||||||
| chr6:106575130 | A | C | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3027T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575130 | |||||||
| chr6:106575136 | G | T | 2 | a0001c0004t0003g0320 a0001c0004t0003g0349 |
2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1084-3033C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575136 | |||||||
| chr6:106575228 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1084-3125C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575228 | |||||||
| chr6:106575247 | C | T | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3144G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575247 | |||||||
| chr6:106575291 | G | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-3188C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575291 | |||||||
| chr6:106575306 | C | T | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3203G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575306 | |||||||
| chr6:106575351 | G | A | 10 | a0001c0001t0005g0358 a0001c0001t0005g0359 a0001c0001t0005g0361 others(7): Show |
10 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-3248C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575351 | |||||||
| chr6:106575384 | C | G | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3281G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575384 | |||||||
| chr6:106575439 | C | T | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1084-3336G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575439 | |||||||
| chr6:106575492 | G | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-3389C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575492 | |||||||
| chr6:106575512 | T | C | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3409A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575512 | |||||||
| chr6:106575527 | CCTCT | C | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3428_1084-342 others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575527 | |||||||
| chr6:106575555 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1084-3452G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575555 | |||||||
| chr6:106575651 | C | T | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3548G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575651 | |||||||
| chr6:106575702 | G | A | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3599C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575702 | |||||||
| chr6:106575853 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1084-3750C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575853 | |||||||
| chr6:106575903 | C | T | 1 | a0001c0005t0008g0355 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1084-3800G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575903 | |||||||
| chr6:106575919 | C | T | 1 | a0001c0001t0005g0360 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1084-3816G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575919 | |||||||
| chr6:106575987 | T | A | 1 | a0001c0002t0004g0285 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1084-3884A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575987 | |||||||
| chr6:106576040 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1084-3937T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576040 | |||||||
| chr6:106576272 | A | G | 1 | a0001c0002t0004g0297 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1084-4169T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576272 | |||||||
| chr6:106576332 | C | T | 31 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(28): Show |
38 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1084-4229G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576332 | |||||||
| chr6:106576352 | C | A | 1 | a0001c0002t0001g0039 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1084-4249G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576352 | |||||||
| chr6:106576364 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1084-4261C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576364 | |||||||
| chr6:106576379 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1084-4276T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576379 | |||||||
| chr6:106576434 | T | C | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1084-4331A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576434 | |||||||
| chr6:106576538 | C | T | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-4435G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576538 | |||||||
| chr6:106576557 | A | G | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-4454T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576557 | |||||||
| chr6:106576694 | C | T | 31 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(28): Show |
38 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1084-4591G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576694 | |||||||
| chr6:106576695 | G | A | 5 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084-4592C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576695 | |||||||
| chr6:106576706 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1084-4603G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576706 | |||||||
| chr6:106576758 | C | T | 350 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(347): Show |
377 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1084-4655G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576758 | |||||||
| chr6:106576891 | C | T | 10 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(7): Show |
10 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-4788G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576891 | |||||||
| chr6:106576924 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1084-4821C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576924 | |||||||
| chr6:106577032 | A | G | 1 | a0001c0002t0001g0043 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1084-4929T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577032 | |||||||
| chr6:106577069 | G | A | 16 | a0001c0001t0005g0358 a0001c0001t0005g0359 a0001c0001t0005g0360 others(13): Show |
16 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-4966C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577069 | |||||||
| chr6:106577242 | T | C | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5139A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577242 | |||||||
| chr6:106577306 | T | A | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5203A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577306 | |||||||
| chr6:106577335 | C | T | 1 | a0001c0001t0005g0361 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1084-5232G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577335 | |||||||
| chr6:106577367 | C | G | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5264G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577367 | |||||||
| chr6:106577392 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1084-5289C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577392 | |||||||
| chr6:106577412 | C | T | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5309G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577412 | |||||||
| chr6:106577447 | C | CA | 20 | a0001c0001t0001g0111 a0001c0001t0001g0133 a0001c0001t0001g0196 others(17): Show |
20 | HG00408.hp2 HG01099.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-5345dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | |||||||
| chr6:106577447 | C | CAA | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0113 others(230): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1084-5346_1084-534 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | |||||||
| chr6:106577447 | C | CAAA | 25 | a0001c0001t0001g0121 a0001c0001t0001g0158 a0001c0001t0001g0180 others(22): Show |
25 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.1084-5347_1084-534 others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | |||||||
| chr6:106577447 | C | CAAAA | 43 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0022 others(40): Show |
45 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1084-5348_1084-534 others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | |||||||
| chr6:106577447 | C | CAAAAA | 18 | a0001c0003t0002g0021 a0001c0003t0002g0038 a0001c0003t0002g0047 others(15): Show |
18 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1084-5349_1084-534 others(9): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | |||||||
| chr6:106577447 | CAAAA | C | 7 | a0001c0003t0002g0013 a0001c0003t0002g0101 a0001c0003t0002g0102 others(4): Show |
8 | HG01891.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1084-5348_1084-534 others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | |||||||
| chr6:106577519 | A | C | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5416T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577519 | |||||||
| chr6:106577551 | A | T | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5448T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577551 | |||||||
| chr6:106577592 | T | C | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-5489A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577592 | |||||||
| chr6:106577608 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1084-5505A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577608 | |||||||
| chr6:106577624 | A | G | 9 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 others(6): Show |
9 | HG01261.hp1 HG02602.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-5521T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577624 | |||||||
| chr6:106577754 | G | A | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1083+5574C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577754 | |||||||
| chr6:106577798 | G | A | 1 | a0001c0004t0003g0356 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1083+5530C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577798 | |||||||
| chr6:106577817 | A | G | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1083+5511T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577817 | |||||||
| chr6:106577874 | G | C | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1083+5454C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577874 | |||||||
| chr6:106577911 | T | C | 62 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(59): Show |
65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1083+5417A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577911 | |||||||
| chr6:106578042 | A | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(313): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1083+5286T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578042 | |||||||
| chr6:106578141 | T | C | 1 | a0001c0005t0008g0355 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1083+5187A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578141 | |||||||
| chr6:106578308 | T | G | 1 | a0001c0002t0001g0039 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1083+5020A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578308 | |||||||
| chr6:106578330 | G | A | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(4): Show |
7 | HG02258.hp1 HG02717.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083+4998C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578330 | |||||||
| chr6:106578448 | G | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(251): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1083+4880C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578448 | |||||||
| chr6:106578555 | A | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1083+4773T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578555 | |||||||
| chr6:106578802 | A | G | 1 | a0001c0001t0007g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1083+4526T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578802 | |||||||
| chr6:106578819 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1083+4509A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578819 | |||||||
| chr6:106578831 | C | T | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1083+4497G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578831 | |||||||
| chr6:106578871 | T | C | 1 | a0001c0004t0003g0356 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1083+4457A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578871 | |||||||
| chr6:106578914 | C | CT | 38 | a0001c0001t0001g0208 a0001c0002t0001g0007 a0001c0002t0001g0010 others(35): Show |
41 | HG00438.hp2 HG00738.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.1083+4413dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578914 | |||||||
| chr6:106578914 | CT | C | 9 | a0001c0001t0001g0123 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
10 | HG00323.hp1 HG01169.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1083+4413delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578914 | |||||||
| chr6:106578914 | CTT | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1083+4412_1083+441 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578914 | |||||||
| chr6:106578948 | A | G | 4 | a0001c0004t0003g0343 a0001c0004t0003g0344 a0001c0004t0003g0345 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+4380T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578948 | |||||||
| chr6:106578974 | C | T | 1 | a0001c0003t0002g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1083+4354G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578974 | |||||||
| chr6:106579158 | C | G | 1 | a0001c0003t0002g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1083+4170G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579158 | |||||||
| chr6:106579185 | G | A | 2 | a0001c0004t0003g0323 a0001c0004t0003g0328 |
2 | NA18955.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1083+4143C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579185 | |||||||
| chr6:106579296 | C | T | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(356): Show |
386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.1083+4032G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579296 | |||||||
| chr6:106579416 | G | A | 2 | a0001c0001t0010g0014 a0001c0001t0010g0116 |
3 | HG02109.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1083+3912C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579416 | |||||||
| chr6:106579460 | C | G | 71 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(68): Show |
74 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.1083+3868G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579460 | |||||||
| chr6:106579535 | T | C | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1083+3793A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579535 | |||||||
| chr6:106579606 | A | G | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(202): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1083+3722T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579606 | |||||||
| chr6:106579622 | T | G | 109 | a0001c0002t0001g0008 a0001c0002t0004g0001 a0001c0002t0004g0016 others(106): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1083+3706A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579622 | |||||||
| chr6:106579682 | T | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(79): Show |
86 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1083+3646A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579682 | |||||||
| chr6:106579714 | T | G | 1 | a0001c0005t0008g0342 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1083+3614A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579714 | |||||||
| chr6:106579730 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1083+3598C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579730 | |||||||
| chr6:106579781 | CT | C | 9 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
9 | HG01099.hp1 HG01258.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+3546delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579781 | |||||||
| chr6:106579834 | G | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0230 a0001c0001t0001g0231 |
3 | HG02109.hp2 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1083+3494C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579834 | |||||||
| chr6:106579964 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1083+3364G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579964 | |||||||
| chr6:106580082 | C | T | 1 | a0001c0004t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1083+3246G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580082 | |||||||
| chr6:106580106 | T | C | 5 | a0001c0003t0002g0056 a0001c0003t0002g0084 a0001c0003t0002g0085 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+3222A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580106 | |||||||
| chr6:106580109 | A | G | 5 | a0001c0003t0002g0056 a0001c0003t0002g0084 a0001c0003t0002g0085 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+3219T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580109 | |||||||
| chr6:106580110 | A | T | 1 | a0001c0002t0001g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1083+3218T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580110 | |||||||
| chr6:106580146 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1083+3182C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580146 | |||||||
| chr6:106580213 | C | CA | 40 | a0001c0001t0001g0115 a0001c0001t0001g0150 a0001c0001t0001g0156 others(37): Show |
42 | HG00544.hp1 HG00642.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1083+3114dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580213 | |||||||
| chr6:106580213 | C | CAA | 53 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(50): Show |
56 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.1083+3113_1083+311 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580213 | |||||||
| chr6:106580213 | C | CAAA | 6 | a0001c0003t0002g0051 a0001c0003t0002g0052 a0001c0003t0002g0053 others(3): Show |
6 | HG02559.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+3112_1083+311 others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580213 | |||||||
| chr6:106580213 | CA | C | 9 | a0001c0001t0001g0195 a0001c0001t0001g0255 a0001c0002t0001g0068 others(6): Show |
9 | HG00323.hp1 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+3114delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580213 | |||||||
| chr6:106580337 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0186 |
2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1083+2991T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580337 | |||||||
| chr6:106580424 | A | C | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1083+2904T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580424 | |||||||
| chr6:106580467 | C | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG02165.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1083+2861G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580467 | |||||||
| chr6:106580471 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1083+2857G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580471 | |||||||
| chr6:106580501 | C | T | 109 | a0001c0002t0001g0008 a0001c0002t0004g0001 a0001c0002t0004g0016 others(106): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1083+2827G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580501 | |||||||
| chr6:106580564 | C | T | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1083+2764G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580564 | |||||||
| chr6:106580603 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1083+2725G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580603 | |||||||
| chr6:106580662 | T | G | 1 | a0001c0004t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1083+2666A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580662 | |||||||
| chr6:106580709 | ACT | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1083+2617_1083+261 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580709 | |||||||
| chr6:106580711 | T | A | 1 | a0001c0001t0001g0266 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1083+2617A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580711 | |||||||
| chr6:106580718 | C | CA | 32 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(29): Show |
39 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1083+2609dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580718 | |||||||
| chr6:106580718 | C | CAA | 3 | a0001c0002t0004g0277 a0001c0002t0004g0287 a0001c0002t0004g0298 |
3 | HG02074.hp1 NA18998.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1083+2608_1083+260 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580718 | |||||||
| chr6:106580722 | G | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1083+2606C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580722 | |||||||
| chr6:106580722 | G | GA | 31 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0152 others(28): Show |
32 | HG00438.hp2 HG00639.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1083+2605dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580722 | |||||||
| chr6:106580738 | C | A | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.1083+2590G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580738 | |||||||
| chr6:106580750 | T | A | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.1083+2578A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580750 | |||||||
| chr6:106580764 | T | C | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.1083+2564A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580764 | |||||||
| chr6:106580964 | T | G | 110 | a0001c0001t0001g0211 a0001c0002t0001g0008 a0001c0002t0004g0001 others(107): Show |
121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1083+2364A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580964 | |||||||
| chr6:106580980 | T | TA | 35 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0005g0358 others(32): Show |
38 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1083+2347dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580980 | |||||||
| chr6:106580980 | TA | T | 76 | a0001c0001t0001g0161 a0001c0001t0001g0238 a0001c0002t0001g0008 others(73): Show |
80 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(77): Show |
intron_variant | MODIFIER | c.1083+2347delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580980 | |||||||
| chr6:106581116 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1083+2212A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581116 | |||||||
| chr6:106581277 | T | A | 1 | a0001c0001t0007g0155 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1083+2051A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581277 | |||||||
| chr6:106581283 | G | A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+2045C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581283 | |||||||
| chr6:106581551 | C | G | 1 | a0001c0005t0008g0355 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1083+1777G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581551 | |||||||
| chr6:106581575 | T | C | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1083+1753A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581575 | |||||||
| chr6:106581643 | A | G | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1083+1685T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581643 | |||||||
| chr6:106581876 | C | A | 1 | a0001c0005t0008g0342 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1083+1452G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581876 | |||||||
| chr6:106581975 | A | G | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1083+1353T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581975 | |||||||
| chr6:106582229 | G | A | 1 | a0001c0002t0004g0291 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1083+1099C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582229 | |||||||
| chr6:106582304 | A | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1083+1024T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582304 | |||||||
| chr6:106582495 | G | A | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1083+833C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582495 | |||||||
| chr6:106582587 | T | TATAAGTC others(41): Show |
1 | a0001c0001t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1083+693_1083+740d others(50): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582587 | |||||||
| chr6:106582592 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1083+736C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582592 | |||||||
| chr6:106582688 | C | G | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1083+640G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582688 | |||||||
| chr6:106582797 | C | T | 109 | a0001c0002t0001g0008 a0001c0002t0004g0001 a0001c0002t0004g0016 others(106): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1083+531G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582797 | |||||||
| chr6:106582817 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1083+511G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582817 | |||||||
| chr6:106583071 | C | T | 1 | a0001c0003t0002g0060 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1083+257G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583071 | |||||||
| chr6:106583097 | G | A | 3 | a0001c0002t0001g0011 a0001c0002t0001g0069 a0001c0002t0001g0078 |
4 | HG01496.hp1 HG01928.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+231C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583097 | |||||||
| chr6:106583104 | C | T | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1083+224G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583104 | |||||||
| chr6:106583124 | T | C | 2 | a0001c0001t0007g0154 a0001c0001t0007g0155 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1083+204A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583124 | |||||||
| chr6:106583179 | G | C | 2 | a0001c0002t0009g0305 a0001c0002t0009g0307 |
2 | HG01243.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1083+149C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583179 | |||||||
| chr6:106583251 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1083+77C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583251 | |||||||
| chr6:106583258 | A | C | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1083+70T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583258 | |||||||
| chr6:106583436 | C | T | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.991-16G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583436 | |||||||
| chr6:106583449 | A | G | 1 | a0001c0002t0001g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.991-29T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583449 | |||||||
| chr6:106583621 | A | C | 1 | a0001c0002t0001g0074 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.991-201T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583621 | |||||||
| chr6:106583785 | T | G | 1 | a0001c0003t0002g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.991-365A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583785 | |||||||
| chr6:106583891 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0250 |
2 | HG00733.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.991-471G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583891 | |||||||
| chr6:106583994 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.991-574G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583994 | |||||||
| chr6:106584007 | A | G | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.991-587T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584007 | |||||||
| chr6:106584045 | T | C | 1 | a0001c0002t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.991-625A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584045 | |||||||
| chr6:106584078 | C | A | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.991-658G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584078 | |||||||
| chr6:106584229 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0206 |
2 | NA18993.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.991-809C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584229 | |||||||
| chr6:106584253 | T | G | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-833A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584253 | |||||||
| chr6:106584485 | G | A | 1 | a0001c0002t0004g0298 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.991-1065C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584485 | |||||||
| chr6:106584487 | G | A | 1 | a0001c0002t0001g0068 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.991-1067C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584487 | |||||||
| chr6:106584543 | T | C | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-1123A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584543 | |||||||
| chr6:106584691 | G | A | 315 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(312): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.991-1271C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584691 | |||||||
| chr6:106585225 | A | C | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.991-1805T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585225 | |||||||
| chr6:106585231 | T | C | 1 | a0001c0003t0002g0046 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.991-1811A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585231 | |||||||
| chr6:106585281 | T | C | 109 | a0001c0002t0001g0008 a0001c0002t0004g0001 a0001c0002t0004g0016 others(106): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.991-1861A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585281 | |||||||
| chr6:106585291 | C | T | 109 | a0001c0002t0001g0008 a0001c0002t0004g0001 a0001c0002t0004g0016 others(106): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.991-1871G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585291 | |||||||
| chr6:106585330 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.991-1910T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585330 | |||||||
| chr6:106585413 | CAGA | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(4): Show |
7 | HG02258.hp1 HG02717.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-1996_991-1994d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585413 | |||||||
| chr6:106585443 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.991-2023C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585443 | |||||||
| chr6:106585542 | A | C | 32 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(29): Show |
39 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.991-2122T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585542 | |||||||
| chr6:106585549 | G | A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-2129C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585549 | |||||||
| chr6:106585594 | A | T | 96 | a0001c0002t0001g0008 a0001c0002t0004g0001 a0001c0002t0004g0016 others(93): Show |
107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.990+2085T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585594 | |||||||
| chr6:106585690 | A | T | 1 | a0001c0003t0002g0037 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.990+1989T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585690 | |||||||
| chr6:106585695 | G | A | 72 | a0001c0002t0001g0008 a0001c0003t0002g0009 a0001c0003t0002g0012 others(69): Show |
76 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(73): Show |
intron_variant | MODIFIER | c.990+1984C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585695 | |||||||
| chr6:106585928 | G | C | 1 | a0001c0002t0004g0301 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.990+1751C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585928 | |||||||
| chr6:106586036 | A | G | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.990+1643T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586036 | |||||||
| chr6:106586041 | C | G | 34 | a0001c0001t0001g0184 a0001c0004t0003g0002 a0001c0004t0003g0005 others(31): Show |
42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.990+1638G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586041 | |||||||
| chr6:106586051 | C | T | 1 | a0001c0003t0002g0050 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.990+1628G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586051 | |||||||
| chr6:106586088 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | NA18947.hp2 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+1591T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586088 | |||||||
| chr6:106586118 | T | C | 21 | a0001c0001t0001g0115 a0001c0001t0001g0156 a0001c0001t0001g0161 others(18): Show |
22 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.990+1561A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586118 | |||||||
| chr6:106586275 | T | C | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.990+1404A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586275 | |||||||
| chr6:106586293 | C | T | 3 | a0001c0002t0004g0287 a0001c0003t0011g0299 a0001c0003t0011g0303 |
3 | NA18942.hp1 NA18998.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.990+1386G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586293 | |||||||
| chr6:106586374 | T | C | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.990+1305A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586374 | |||||||
| chr6:106586382 | G | GT | 18 | a0001c0001t0001g0136 a0001c0001t0001g0164 a0001c0001t0001g0181 others(15): Show |
18 | HG02135.hp2 HG02257.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.990+1296dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586382 | |||||||
| chr6:106586661 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.990+1018G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586661 | |||||||
| chr6:106586826 | C | T | 29 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0021 others(26): Show |
31 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.990+853G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586826 | |||||||
| chr6:106586913 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.990+766A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586913 | |||||||
| chr6:106586914 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.990+765C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586914 | |||||||
| chr6:106587010 | C | A | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.990+669G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587010 | |||||||
| chr6:106587037 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.990+642G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587037 | |||||||
| chr6:106587111 | G | A | 55 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0135 others(52): Show |
55 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.990+568C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587111 | |||||||
| chr6:106587135 | C | T | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.990+544G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587135 | |||||||
| chr6:106587189 | G | C | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.990+490C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587189 | |||||||
| chr6:106587319 | G | T | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.990+360C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587319 | |||||||
| chr6:106587576 | C | T | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.990+103G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587576 | |||||||
| chr6:106587914 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0186 |
2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.807-52A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106587914 | |||||||
| chr6:106587991 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.807-129C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106587991 | |||||||
| chr6:106588055 | T | C | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-193A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588055 | |||||||
| chr6:106588197 | CA | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-336delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588197 | |||||||
| chr6:106588353 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(313): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.807-491T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588353 | |||||||
| chr6:106588456 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-594C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588456 | |||||||
| chr6:106588466 | C | T | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 |
3 | HG02258.hp1 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.807-604G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588466 | |||||||
| chr6:106588516 | C | CAAAAAAA others(340): Show |
1 | a0001c0004t0003g0353 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.807-655_807-654ins others(347): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588516 | |||||||
| chr6:106588686 | G | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-824C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588686 | |||||||
| chr6:106588771 | A | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-909T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588771 | |||||||
| chr6:106588782 | C | T | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.807-920G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588782 | |||||||
| chr6:106588829 | G | C | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.807-967C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588829 | |||||||
| chr6:106588881 | C | T | 34 | a0001c0001t0001g0184 a0001c0004t0003g0002 a0001c0004t0003g0005 others(31): Show |
42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.807-1019G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588881 | |||||||
| chr6:106589006 | A | G | 1 | a0001c0002t0001g0043 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.807-1144T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589006 | |||||||
| chr6:106589034 | C | T | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.807-1172G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589034 | |||||||
| chr6:106589058 | C | T | 1 | a0001c0002t0001g0065 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.807-1196G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589058 | |||||||
| chr6:106589098 | G | A | 2 | a0001c0003t0002g0094 a0001c0003t0002g0095 |
2 | HG00639.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.807-1236C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589098 | |||||||
| chr6:106589102 | C | T | 5 | a0001c0001t0001g0122 a0001c0001t0001g0188 a0001c0001t0001g0200 others(2): Show |
5 | HG02135.hp1 NA18993.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.807-1240G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589102 | |||||||
| chr6:106589104 | C | CAGAAGAA others(8): Show |
21 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0033 others(18): Show |
22 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(19): Show |
intron_variant | MODIFIER | c.807-1257_807-1243d others(17): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589104 | |||||||
| chr6:106589104 | CAGA | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1245_807-1243d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589104 | |||||||
| chr6:106589126 | GGAA | G | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-1267_807-1265d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589126 | |||||||
| chr6:106589177 | AGGAGGAG others(3): Show |
A | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.807-1325_807-1316d others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589177 | |||||||
| chr6:106589186 | A | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1324T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589186 | |||||||
| chr6:106589187 | G | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1325C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589187 | |||||||
| chr6:106589191 | GGA | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1331_807-1330d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589191 | |||||||
| chr6:106589213 | G | GGGA | 8 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0034 others(5): Show |
9 | NA18950.hp2 NA18971.hp2 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-1354_807-1352d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589213 | |||||||
| chr6:106589219 | A | G | 7 | a0001c0001t0001g0177 a0001c0001t0001g0238 a0001c0001t0001g0239 others(4): Show |
7 | HG00639.hp1 HG00738.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.807-1357T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589219 | |||||||
| chr6:106589225 | G | A | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(266): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.807-1363C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589225 | |||||||
| chr6:106589226 | A | G | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(266): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.807-1364T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589226 | |||||||
| chr6:106589229 | A | G | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.807-1367T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589229 | |||||||
| chr6:106589234 | G | GAGGGAGG others(257): Show |
1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-1373_807-1372i others(266): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589234 | |||||||
| chr6:106589237 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-1375C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGACGAGG others(326): Show |
1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(335): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(406): Show |
1 | a0001c0001t0005g0368 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(415): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(365): Show |
1 | a0001c0001t0001g0164 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(374): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(349): Show |
2 | a0001c0001t0001g0117 a0001c0001t0001g0171 |
2 | NA19009.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(358): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(329): Show |
1 | a0001c0001t0001g0234 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(338): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(366): Show |
1 | a0001c0001t0001g0182 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(375): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(330): Show |
1 | a0001c0001t0001g0198 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(339): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(356): Show |
16 | a0001c0001t0001g0004 a0001c0001t0001g0121 a0001c0001t0001g0129 others(13): Show |
18 | HG00438.hp1 HG00597.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(365): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(368): Show |
1 | a0001c0001t0001g0220 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(377): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(312): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0235 |
2 | HG00280.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(321): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(354): Show |
1 | a0001c0001t0001g0113 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(363): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(369): Show |
46 | a0001c0001t0001g0003 a0001c0001t0001g0111 a0001c0001t0001g0118 others(43): Show |
48 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(378): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(369): Show |
2 | a0001c0001t0001g0205 a0001c0001t0001g0219 |
2 | NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(378): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(369): Show |
1 | a0001c0001t0001g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(378): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(370): Show |
1 | a0001c0001t0001g0190 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(371): Show |
1 | a0001c0001t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(380): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(359): Show |
1 | a0001c0001t0001g0228 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(368): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(370): Show |
1 | a0001c0001t0001g0209 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(396): Show |
1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(405): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(389): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0213 |
3 | HG00408.hp2 NA18999.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(398): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(373): Show |
1 | a0001c0001t0001g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(382): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(349): Show |
1 | a0001c0001t0001g0181 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(358): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(349): Show |
1 | a0001c0001t0001g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(358): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(371): Show |
1 | a0001c0001t0001g0132 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(380): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(357): Show |
1 | a0001c0001t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(366): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(228): Show |
9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(237): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(231): Show |
1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(240): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(176): Show |
1 | a0001c0003t0002g0036 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(185): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(191): Show |
20 | a0001c0003t0002g0033 a0001c0003t0002g0037 a0001c0003t0002g0045 others(17): Show |
20 | HG01891.hp2 HG02074.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(200): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(206): Show |
2 | a0001c0003t0002g0053 a0001c0003t0002g0054 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(215): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(167): Show |
2 | a0001c0003t0002g0100 a0001c0003t0002g0103 |
2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(176): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(182): Show |
26 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0021 others(23): Show |
28 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(191): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(377): Show |
1 | a0001c0002t0001g0042 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(386): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(212): Show |
1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(221): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(297): Show |
1 | a0001c0002t0004g0279 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(306): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(346): Show |
1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(355): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(359): Show |
1 | a0001c0002t0001g0078 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(368): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(338): Show |
1 | a0001c0002t0001g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(347): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(330): Show |
2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG00735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(339): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(345): Show |
1 | a0001c0001t0001g0252 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(354): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(350): Show |
1 | a0001c0001t0001g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(359): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(350): Show |
1 | a0001c0001t0001g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(359): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(365): Show |
1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(374): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(375): Show |
3 | a0001c0002t0001g0066 a0001c0002t0001g0067 a0001c0002t0001g0077 |
3 | HG02451.hp1 HG02976.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(384): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(367): Show |
4 | a0001c0001t0001g0146 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | NA18947.hp2 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(376): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(358): Show |
1 | a0001c0002t0001g0075 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(367): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(358): Show |
1 | a0001c0002t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(367): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(343): Show |
1 | a0004c0007t0001g0081 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(352): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(358): Show |
18 | a0001c0001t0001g0208 a0001c0002t0001g0007 a0001c0002t0001g0010 others(15): Show |
21 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(367): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(358): Show |
2 | a0001c0004t0003g0313 a0001c0004t0003g0314 |
2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(367): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(365): Show |
1 | a0001c0001t0001g0169 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(374): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(371): Show |
1 | a0001c0002t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(380): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(350): Show |
35 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0135 others(32): Show |
35 | HG00140.hp2 HG00733.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(359): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(365): Show |
2 | a0001c0001t0001g0240 a0001c0001t0001g0274 |
2 | HG00323.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(374): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(363): Show |
1 | a0001c0001t0001g0259 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(372): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(370): Show |
1 | a0001c0001t0001g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(370): Show |
1 | a0001c0001t0001g0266 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(370): Show |
1 | a0001c0001t0001g0140 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(398): Show |
1 | a0001c0002t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(407): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(380): Show |
1 | a0001c0001t0001g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(389): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(415): Show |
5 | a0001c0001t0005g0359 a0001c0001t0005g0361 a0001c0001t0005g0362 others(2): Show |
5 | HG01099.hp2 HG02258.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(424): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(441): Show |
1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(450): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(425): Show |
3 | a0001c0001t0005g0358 a0001c0001t0007g0114 a0001c0001t0007g0153 |
3 | HG00544.hp1 HG01175.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(434): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(354): Show |
1 | a0001c0001t0001g0172 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(363): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(402): Show |
1 | a0001c0001t0001g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(411): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(331): Show |
1 | a0001c0001t0001g0248 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(340): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(405): Show |
1 | a0001c0001t0005g0367 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(414): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(350): Show |
5 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG02602.hp1 HG02698.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(359): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(405): Show |
1 | a0001c0001t0010g0014 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(414): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(405): Show |
1 | a0001c0001t0005g0360 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(414): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(410): Show |
2 | a0001c0001t0007g0154 a0001c0001t0007g0155 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(419): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(416): Show |
1 | a0001c0001t0010g0116 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(425): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(385): Show |
2 | a0001c0001t0005g0363 a0001c0001t0005g0364 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(394): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(362): Show |
1 | a0001c0002t0001g0039 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(371): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(194): Show |
7 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0034 others(4): Show |
8 | NA18950.hp2 NA18971.hp2 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(203): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(172): Show |
1 | a0001c0003t0002g0089 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(181): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(201): Show |
1 | a0001c0003t0002g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(210): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(277): Show |
1 | a0001c0002t0004g0278 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(286): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(297): Show |
1 | a0001c0002t0004g0276 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(306): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(267): Show |
1 | a0001c0002t0004g0295 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(276): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(272): Show |
1 | a0001c0002t0004g0290 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(281): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(287): Show |
21 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(18): Show |
28 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(296): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(275): Show |
1 | a0001c0002t0004g0291 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(284): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(288): Show |
1 | a0001c0002t0004g0280 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(288): Show |
1 | a0001c0002t0004g0292 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(288): Show |
1 | a0001c0002t0004g0296 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(288): Show |
1 | a0001c0002t0004g0286 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(307): Show |
1 | a0001c0002t0004g0301 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(316): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(336): Show |
1 | a0001c0001t0001g0269 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(345): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(288): Show |
1 | a0001c0002t0004g0293 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(346): Show |
2 | a0001c0001t0001g0270 a0001c0001t0001g0272 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(355): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(373): Show |
1 | a0001c0002t0001g0064 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(382): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGAGG others(415): Show |
1 | a0001c0001t0007g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(424): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGAGGGAG others(372): Show |
1 | a0001c0002t0001g0043 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(381): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGGAGGAG others(158): Show |
8 | a0001c0004t0003g0005 a0001c0004t0003g0315 a0001c0004t0003g0317 others(5): Show |
10 | HG00609.hp2 HG02083.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(167): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGGAGGAG others(159): Show |
38 | a0001c0001t0001g0015 a0001c0001t0001g0120 a0001c0001t0001g0152 others(35): Show |
45 | HG00423.hp2 HG00544.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(168): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGGAGGAG others(160): Show |
1 | a0001c0004t0003g0325 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(169): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGGAGGAG others(146): Show |
1 | a0001c0004t0003g0344 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(155): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGGAGGAG others(160): Show |
1 | a0001c0004t0003g0340 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(169): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGGGGAGG others(382): Show |
2 | a0001c0002t0009g0306 a0001c0002t0009g0308 |
2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(391): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589237 | G | GGGGGAGG others(382): Show |
2 | a0001c0002t0009g0305 a0001c0002t0009g0307 |
2 | HG01243.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(391): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | |||||||
| chr6:106589238 | G | GGAGGAGG others(221): Show |
1 | a0001c0004t0003g0347 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.807-1377_807-1376i others(230): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589238 | |||||||
| chr6:106589242 | G | A | 21 | a0001c0001t0001g0115 a0001c0001t0001g0156 a0001c0001t0001g0161 others(18): Show |
22 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.807-1380C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589242 | |||||||
| chr6:106589251 | A | AAGG | 39 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(36): Show |
46 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.807-1392_807-1390d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589251 | |||||||
| chr6:106589251 | A | G | 1 | a0001c0004t0003g0347 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.807-1389T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589251 | |||||||
| chr6:106589263 | A | AAGAAGGA others(32): Show |
1 | a0001c0001t0001g0198 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.807-1402_807-1401i others(41): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589263 | |||||||
| chr6:106589266 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0198 |
2 | HG01257.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.807-1404C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589266 | |||||||
| chr6:106589269 | A | G | 2 | a0001c0003t0002g0100 a0001c0003t0002g0103 |
2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.807-1407T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589269 | |||||||
| chr6:106589272 | A | G | 2 | a0001c0003t0002g0100 a0001c0003t0002g0103 |
2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.807-1410T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589272 | |||||||
| chr6:106589275 | A | G | 2 | a0001c0001t0001g0140 a0001c0002t0001g0008 |
3 | HG03453.hp1 NA18747.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.807-1413T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589275 | |||||||
| chr6:106589278 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0261 a0001c0002t0001g0008 |
4 | HG03453.hp1 HG03704.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.807-1416C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589278 | |||||||
| chr6:106589278 | G | GAGA | 268 | a0001c0001t0001g0004 a0001c0001t0001g0111 a0001c0001t0001g0113 others(265): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.807-1419_807-1417d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589278 | |||||||
| chr6:106589278 | G | GAGAAGAA others(8): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
6 | NA18952.hp2 NA18978.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.807-1417_807-1416i others(17): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589278 | |||||||
| chr6:106589289 | A | G | 39 | a0001c0001t0001g0206 a0001c0002t0004g0001 a0001c0002t0004g0016 others(36): Show |
46 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.807-1427T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589289 | |||||||
| chr6:106589290 | G | A | 38 | a0001c0001t0001g0206 a0001c0002t0004g0001 a0001c0002t0004g0016 others(35): Show |
45 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.807-1428C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589290 | |||||||
| chr6:106589292 | G | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1430C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589292 | |||||||
| chr6:106589293 | A | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1431T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589293 | |||||||
| chr6:106589303 | G | A | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1441C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589303 | |||||||
| chr6:106589304 | G | A | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1442C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589304 | |||||||
| chr6:106589305 | A | G | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1443T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589305 | |||||||
| chr6:106589306 | G | A | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1444C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589306 | |||||||
| chr6:106589309 | G | A | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1447C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589309 | |||||||
| chr6:106589312 | G | A | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1450C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589312 | |||||||
| chr6:106589315 | G | A | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1453C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589315 | |||||||
| chr6:106589318 | A | G | 2 | a0001c0001t0001g0206 a0001c0003t0002g0100 |
2 | HG02055.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.807-1456T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589318 | |||||||
| chr6:106589321 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.807-1459C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589321 | |||||||
| chr6:106589324 | A | G | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1462T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589324 | |||||||
| chr6:106589327 | A | G | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1465T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589327 | |||||||
| chr6:106589398 | C | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-1536G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589398 | |||||||
| chr6:106589596 | C | T | 1 | a0001c0002t0001g0075 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.807-1734G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589596 | |||||||
| chr6:106589712 | C | T | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.807-1850G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589712 | |||||||
| chr6:106589790 | A | G | 1 | a0001c0002t0004g0287 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.807-1928T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589790 | |||||||
| chr6:106589834 | C | T | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-1972G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589834 | |||||||
| chr6:106589938 | C | T | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.807-2076G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589938 | |||||||
| chr6:106589968 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.807-2106T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589968 | |||||||
| chr6:106590112 | G | T | 1 | a0001c0004t0003g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.806+2052C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590112 | |||||||
| chr6:106590126 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.806+2038G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590126 | |||||||
| chr6:106590272 | G | A | 2 | a0001c0002t0001g0108 a0001c0003t0002g0052 |
2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.806+1892C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590272 | |||||||
| chr6:106590445 | G | T | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.806+1719C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590445 | |||||||
| chr6:106590450 | T | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(251): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.806+1714A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590450 | |||||||
| chr6:106590468 | G | A | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.806+1696C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590468 | |||||||
| chr6:106590531 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.806+1633T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590531 | |||||||
| chr6:106590579 | G | C | 1 | a0001c0002t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.806+1585C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590579 | |||||||
| chr6:106590606 | T | C | 1 | a0001c0001t0007g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.806+1558A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590606 | |||||||
| chr6:106590652 | T | A | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.806+1512A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590652 | |||||||
| chr6:106590693 | C | T | 22 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0033 others(19): Show |
23 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(20): Show |
intron_variant | MODIFIER | c.806+1471G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590693 | |||||||
| chr6:106590714 | C | CA | 6 | a0001c0002t0004g0286 a0001c0003t0002g0038 a0001c0003t0002g0098 others(3): Show |
6 | HG01884.hp1 NA18963.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+1449dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | |||||||
| chr6:106590714 | C | CAA | 85 | a0001c0002t0001g0044 a0001c0002t0001g0069 a0001c0002t0004g0001 others(82): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.806+1448_806+1449d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | |||||||
| chr6:106590714 | C | CAAA | 39 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0165 others(36): Show |
42 | HG00280.hp1 HG00438.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.806+1447_806+1449d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | |||||||
| chr6:106590714 | C | CAAAA | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(129): Show |
137 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.806+1446_806+1449d others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | |||||||
| chr6:106590714 | C | CAAAAA | 24 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0136 others(21): Show |
24 | HG00140.hp1 HG01074.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.806+1445_806+1449d others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | |||||||
| chr6:106590714 | C | CAAAAAA | 29 | a0001c0001t0001g0115 a0001c0001t0001g0139 a0001c0001t0001g0143 others(26): Show |
30 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.806+1444_806+1449d others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | |||||||
| chr6:106590783 | G | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(214): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.806+1381C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590783 | |||||||
| chr6:106590796 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.806+1368C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590796 | |||||||
| chr6:106590809 | C | G | 1 | a0001c0003t0002g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.806+1355G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590809 | |||||||
| chr6:106590839 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.806+1325C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590839 | |||||||
| chr6:106590846 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.806+1318G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590846 | |||||||
| chr6:106590847 | G | A | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.806+1317C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590847 | |||||||
| chr6:106590908 | G | A | 1 | a0001c0003t0002g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.806+1256C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590908 | |||||||
| chr6:106590993 | A | T | 1 | a0001c0004t0003g0351 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.806+1171T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590993 | |||||||
| chr6:106591051 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0224 |
2 | NA18998.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.806+1113G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591051 | |||||||
| chr6:106591210 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(85): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.806+954G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591210 | |||||||
| chr6:106591349 | C | T | 5 | a0001c0003t0002g0056 a0001c0003t0002g0084 a0001c0003t0002g0085 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.806+815G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591349 | |||||||
| chr6:106591393 | G | C | 1 | a0001c0004t0003g0335 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.806+771C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591393 | |||||||
| chr6:106591420 | C | CTT | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.806+742_806+743dup others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591420 | |||||||
| chr6:106591429 | C | T | 1 | a0001c0003t0002g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.806+735G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591429 | |||||||
| chr6:106591430 | T | C | 1 | a0001c0003t0002g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.806+734A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591430 | |||||||
| chr6:106591443 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.806+721A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591443 | |||||||
| chr6:106591553 | C | T | 55 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0135 others(52): Show |
55 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.806+611G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591553 | |||||||
| chr6:106591575 | A | T | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.806+589T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591575 | |||||||
| chr6:106591580 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.806+584C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591580 | |||||||
| chr6:106591652 | C | T | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.806+512G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591652 | |||||||
| chr6:106591699 | T | A | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.806+465A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591699 | |||||||
| chr6:106591699 | T | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.806+465A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591699 | |||||||
| chr6:106591845 | G | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.806+319C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591845 | |||||||
| chr6:106592304 | C | T | 1 | a0001c0002t0001g0075 | 1 | HG02523.hp2 | splice_region_variant&intron_variant | LOW | c.670-4G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592304 | |||||||
| chr6:106592386 | T | C | 1 | a0001c0002t0001g0074 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.670-86A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592386 | |||||||
| chr6:106592415 | G | A | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.670-115C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592415 | |||||||
| chr6:106592428 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.670-128C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592428 | |||||||
| chr6:106592588 | G | A | 1 | a0001c0003t0002g0022 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.670-288C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592588 | |||||||
| chr6:106592645 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0271 |
2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.670-345G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592645 | |||||||
| chr6:106592657 | C | T | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.670-357G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592657 | |||||||
| chr6:106592690 | G | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-390C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592690 | |||||||
| chr6:106592929 | C | CA | 38 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(35): Show |
45 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.670-630dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592929 | |||||||
| chr6:106592936 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.670-636T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592936 | |||||||
| chr6:106593093 | C | T | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-793G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593093 | |||||||
| chr6:106593099 | G | C | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.670-799C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593099 | |||||||
| chr6:106593100 | C | T | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.670-800G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593100 | |||||||
| chr6:106593201 | T | C | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.670-901A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593201 | |||||||
| chr6:106593327 | A | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.670-1027T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593327 | |||||||
| chr6:106593418 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670-1118C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593418 | |||||||
| chr6:106593493 | A | C | 2 | a0001c0003t0002g0091 a0001c0003t0002g0096 |
2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.670-1193T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593493 | |||||||
| chr6:106593547 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1247A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593547 | |||||||
| chr6:106593552 | A | C | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1252T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593552 | |||||||
| chr6:106593556 | G | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1256C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593556 | |||||||
| chr6:106593558 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1258A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593558 | |||||||
| chr6:106593559 | A | T | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1259T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593559 | |||||||
| chr6:106593568 | C | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1268G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593568 | |||||||
| chr6:106593570 | C | T | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1270G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593570 | |||||||
| chr6:106593573 | G | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1273C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593573 | |||||||
| chr6:106593576 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1276A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593576 | |||||||
| chr6:106593578 | C | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1278G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593578 | |||||||
| chr6:106593580 | AGGGATCT others(52): Show |
A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1339_670-1281d others(61): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593580 | |||||||
| chr6:106593642 | G | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1342C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593642 | |||||||
| chr6:106593643 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1343A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593643 | |||||||
| chr6:106593647 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1347A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593647 | |||||||
| chr6:106593648 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1348A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593648 | |||||||
| chr6:106593649 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1349A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593649 | |||||||
| chr6:106593650 | C | T | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1350G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593650 | |||||||
| chr6:106593651 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1351A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593651 | |||||||
| chr6:106593652 | G | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1352C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593652 | |||||||
| chr6:106593653 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1353A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593653 | |||||||
| chr6:106593654 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1354A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593654 | |||||||
| chr6:106593660 | C | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1360G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593660 | |||||||
| chr6:106593665 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1365A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593665 | |||||||
| chr6:106593667 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1367A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593667 | |||||||
| chr6:106593671 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1371A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593671 | |||||||
| chr6:106593672 | A | G | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1372T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593672 | |||||||
| chr6:106593676 | G | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1376C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593676 | |||||||
| chr6:106593677 | G | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1377C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593677 | |||||||
| chr6:106593678 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1378A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593678 | |||||||
| chr6:106593679 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1379A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593679 | |||||||
| chr6:106593680 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1380A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593680 | |||||||
| chr6:106593681 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1381A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593681 | |||||||
| chr6:106593682 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1382A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593682 | |||||||
| chr6:106593689 | T | TAAAAAAA others(59): Show |
1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1390_670-1389i others(68): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593689 | |||||||
| chr6:106593693 | T | A | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1393A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593693 | |||||||
| chr6:106593694 | A | T | 1 | a0001c0003t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1394T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593694 | |||||||
| chr6:106593779 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.670-1479T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593779 | |||||||
| chr6:106593846 | G | A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.670-1546C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593846 | |||||||
| chr6:106593880 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-1580T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593880 | |||||||
| chr6:106594068 | T | C | 1 | a0001c0004t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.670-1768A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594068 | |||||||
| chr6:106594081 | G | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.670-1781C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594081 | |||||||
| chr6:106594229 | G | A | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.670-1929C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594229 | |||||||
| chr6:106594326 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.670-2026T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594326 | |||||||
| chr6:106594384 | C | T | 1 | a0005c0010t0002g0110 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.670-2084G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594384 | |||||||
| chr6:106594438 | G | A | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-2138C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594438 | |||||||
| chr6:106594491 | C | G | 1 | a0001c0004t0003g0323 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.670-2191G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594491 | |||||||
| chr6:106594527 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0001g0272 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.670-2227T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594527 | |||||||
| chr6:106594527 | AAAAG | A | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-2231_670-2228d others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594527 | |||||||
| chr6:106594537 | A | C | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.670-2237T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594537 | |||||||
| chr6:106594579 | C | A | 306 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(303): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.670-2279G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594579 | |||||||
| chr6:106594691 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-2391A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594691 | |||||||
| chr6:106594794 | T | C | 1 | a0001c0004t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.670-2494A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594794 | |||||||
| chr6:106594846 | G | A | 1 | a0001c0001t0007g0114 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.670-2546C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594846 | |||||||
| chr6:106594988 | T | G | 315 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(312): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.670-2688A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594988 | |||||||
| chr6:106595052 | T | G | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-2752A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595052 | |||||||
| chr6:106595055 | G | A | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.670-2755C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595055 | |||||||
| chr6:106595065 | A | G | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(251): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.670-2765T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595065 | |||||||
| chr6:106595116 | A | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.670-2816T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595116 | |||||||
| chr6:106595134 | T | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02523.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.670-2834A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595134 | |||||||
| chr6:106595150 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-2850A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595150 | |||||||
| chr6:106595194 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-2894A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595194 | |||||||
| chr6:106595287 | C | A | 17 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(14): Show |
20 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.670-2987G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595287 | |||||||
| chr6:106595327 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.670-3027T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595327 | |||||||
| chr6:106595408 | A | G | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.670-3108T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595408 | |||||||
| chr6:106595419 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.670-3119G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595419 | |||||||
| chr6:106595496 | CTTTCT | C | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-3201_670-3197d others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595496 | |||||||
| chr6:106595500 | C | CT | 6 | a0001c0003t0002g0033 a0001c0003t0002g0051 a0001c0003t0002g0088 others(3): Show |
6 | HG00544.hp2 HG02559.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-3201dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595500 | |||||||
| chr6:106595500 | CT | C | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(200): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.670-3201delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595500 | |||||||
| chr6:106595500 | CTT | C | 34 | a0001c0001t0001g0164 a0001c0002t0004g0001 a0001c0002t0004g0016 others(31): Show |
41 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.670-3202_670-3201d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595500 | |||||||
| chr6:106595521 | G | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-3221C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595521 | |||||||
| chr6:106595558 | C | T | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(202): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.670-3258G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595558 | |||||||
| chr6:106595623 | G | A | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.670-3323C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595623 | |||||||
| chr6:106595631 | GAGATTAC others(1): Show |
G | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-3339_670-3332d others(10): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595631 | |||||||
| chr6:106595632 | A | G | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(246): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.670-3332T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595632 | |||||||
| chr6:106595642 | T | A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-3342A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595642 | |||||||
| chr6:106595686 | A | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(250): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.670-3386T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595686 | |||||||
| chr6:106595823 | C | T | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-3523G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595823 | |||||||
| chr6:106595872 | A | C | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-3572T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595872 | |||||||
| chr6:106595876 | A | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(250): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.670-3576T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595876 | |||||||
| chr6:106595894 | C | G | 1 | a0001c0002t0004g0283 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.670-3594G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595894 | |||||||
| chr6:106596038 | CATT | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(202): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.670-3741_670-3739d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596038 | |||||||
| chr6:106596061 | C | T | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(313): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.670-3761G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596061 | |||||||
| chr6:106596206 | TAAG | T | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(202): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.670-3909_670-3907d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596206 | |||||||
| chr6:106596318 | A | G | 1 | a0001c0003t0002g0104 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.670-4018T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596318 | |||||||
| chr6:106596366 | T | C | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.670-4066A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596366 | |||||||
| chr6:106596400 | C | G | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.670-4100G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596400 | |||||||
| chr6:106596426 | G | A | 1 | a0001c0002t0001g0068 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.670-4126C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596426 | |||||||
| chr6:106596429 | A | G | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.670-4129T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596429 | |||||||
| chr6:106596667 | A | C | 61 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(58): Show |
64 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.670-4367T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596667 | |||||||
| chr6:106596798 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.670-4498G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596798 | |||||||
| chr6:106596957 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-4657A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596957 | |||||||
| chr6:106596981 | C | T | 11 | a0001c0001t0005g0358 a0001c0001t0005g0359 a0001c0001t0005g0360 others(8): Show |
11 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.670-4681G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596981 | |||||||
| chr6:106597135 | T | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-4835A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597135 | |||||||
| chr6:106597217 | T | C | 2 | a0001c0004t0003g0344 a0001c0004t0003g0346 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.670-4917A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597217 | |||||||
| chr6:106597298 | A | C | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-4998T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597298 | |||||||
| chr6:106597301 | T | C | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-5001A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597301 | |||||||
| chr6:106597339 | C | A | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(356): Show |
386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.670-5039G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597339 | |||||||
| chr6:106597564 | G | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670-5264C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597564 | |||||||
| chr6:106597565 | AATCGCTG others(1729): Show |
A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3573_670-5266d others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597565 | |||||||
| chr6:106597625 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+5249C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597625 | |||||||
| chr6:106597691 | C | CT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0121 a0001c0001t0001g0170 others(5): Show |
8 | HG02572.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+5182dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597691 | |||||||
| chr6:106597691 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.669+5183G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597691 | |||||||
| chr6:106597702 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0201 |
2 | NA18986.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.669+5172A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597702 | |||||||
| chr6:106597740 | A | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+5134T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597740 | |||||||
| chr6:106597784 | C | T | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.669+5090G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597784 | |||||||
| chr6:106597829 | A | G | 1 | a0001c0004t0003g0323 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.669+5045T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597829 | |||||||
| chr6:106597830 | C | T | 99 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(96): Show |
109 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.669+5044G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597830 | |||||||
| chr6:106597854 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+5020G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597854 | |||||||
| chr6:106597993 | A | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(85): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.669+4881T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597993 | |||||||
| chr6:106598017 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.669+4857C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598017 | |||||||
| chr6:106598020 | T | C | 1 | a0001c0002t0001g0069 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.669+4854A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598020 | |||||||
| chr6:106598050 | A | G | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.669+4824T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598050 | |||||||
| chr6:106598072 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.669+4802T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598072 | |||||||
| chr6:106598132 | T | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+4742A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598132 | |||||||
| chr6:106598145 | G | A | 5 | a0001c0001t0001g0264 a0001c0005t0008g0310 a0001c0005t0008g0311 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+4729C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598145 | |||||||
| chr6:106598166 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.669+4708C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598166 | |||||||
| chr6:106598309 | C | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+4565G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598309 | |||||||
| chr6:106598351 | G | A | 1 | a0001c0003t0002g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.669+4523C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598351 | |||||||
| chr6:106598413 | T | C | 1 | a0001c0005t0008g0310 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.669+4461A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598413 | |||||||
| chr6:106598447 | T | C | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.669+4427A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598447 | |||||||
| chr6:106598454 | G | T | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+4420C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598454 | |||||||
| chr6:106598620 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0221 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.669+4254G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598620 | |||||||
| chr6:106598651 | G | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(85): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.669+4223C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598651 | |||||||
| chr6:106598836 | C | T | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+4038G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598836 | |||||||
| chr6:106598941 | C | T | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+3933G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598941 | |||||||
| chr6:106599027 | ATTTAT | A | 5 | a0001c0003t0002g0013 a0001c0003t0002g0101 a0001c0003t0002g0102 others(2): Show |
6 | HG01891.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+3842_669+3846d others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599027 | |||||||
| chr6:106599317 | A | G | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3557T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599317 | |||||||
| chr6:106599319 | C | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3555G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599319 | |||||||
| chr6:106599323 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3551A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599323 | |||||||
| chr6:106599325 | T | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3549A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599325 | |||||||
| chr6:106599326 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3548A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599326 | |||||||
| chr6:106599331 | T | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3543A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599331 | |||||||
| chr6:106599338 | T | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3536A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599338 | |||||||
| chr6:106599341 | T | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3533A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599341 | |||||||
| chr6:106599342 | C | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3532G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599342 | |||||||
| chr6:106599347 | T | G | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3527A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599347 | |||||||
| chr6:106599352 | A | G | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3522T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599352 | |||||||
| chr6:106599354 | T | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3520A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599354 | |||||||
| chr6:106599355 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3519A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599355 | |||||||
| chr6:106599356 | A | T | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3518T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599356 | |||||||
| chr6:106599358 | A | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(179): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.669+3516T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599358 | |||||||
| chr6:106599360 | T | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3514A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599360 | |||||||
| chr6:106599362 | C | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3512G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599362 | |||||||
| chr6:106599365 | CCTGTGTC others(1930): Show |
C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1572_669+3508d others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599365 | |||||||
| chr6:106599448 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.669+3426A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599448 | |||||||
| chr6:106599451 | C | CT | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(206): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.669+3422dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599451 | |||||||
| chr6:106599460 | T | C | 4 | a0001c0005t0008g0310 a0001c0005t0008g0311 a0001c0005t0008g0318 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+3414A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599460 | |||||||
| chr6:106599502 | C | T | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+3372G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599502 | |||||||
| chr6:106599545 | G | C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(248): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.669+3329C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599545 | |||||||
| chr6:106599561 | T | TTGCATCT others(339): Show |
1 | a0001c0001t0001g0140 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.669+3312_669+3313i others(348): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599561 | |||||||
| chr6:106599596 | G | A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+3278C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599596 | |||||||
| chr6:106599680 | T | A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+3194A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599680 | |||||||
| chr6:106599684 | C | T | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+3190G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599684 | |||||||
| chr6:106599710 | T | C | 1 | a0001c0002t0001g0007 | 2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.669+3164A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599710 | |||||||
| chr6:106599772 | T | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(211): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.669+3102A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599772 | |||||||
| chr6:106599773 | G | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0238 a0001c0001t0001g0247 |
3 | HG01934.hp2 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.669+3101C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599773 | |||||||
| chr6:106599835 | C | T | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+3039G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599835 | |||||||
| chr6:106599835 | CCTT | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
42 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.669+3036_669+3038d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599835 | |||||||
| chr6:106599836 | C | CT | 11 | a0001c0001t0001g0123 a0001c0001t0001g0165 a0001c0003t0006g0023 others(8): Show |
11 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+3037dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599836 | |||||||
| chr6:106599836 | C | T | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+3038G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599836 | |||||||
| chr6:106599836 | CT | C | 6 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0201 others(3): Show |
6 | HG02523.hp2 HG02572.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+3037delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599836 | |||||||
| chr6:106599998 | G | A | 21 | a0001c0001t0001g0115 a0001c0001t0001g0156 a0001c0001t0001g0161 others(18): Show |
22 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.669+2876C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599998 | |||||||
| chr6:106600014 | T | A | 1 | a0001c0002t0001g0075 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.669+2860A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600014 | |||||||
| chr6:106600067 | A | G | 59 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(56): Show |
62 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.669+2807T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600067 | |||||||
| chr6:106600088 | C | G | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+2786G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600088 | |||||||
| chr6:106600090 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | NA18947.hp2 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+2784G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600090 | |||||||
| chr6:106600095 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.669+2779G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600095 | |||||||
| chr6:106600148 | T | C | 1 | a0001c0005t0008g0355 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+2726A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600148 | |||||||
| chr6:106600167 | G | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(211): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.669+2707C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600167 | |||||||
| chr6:106600168 | G | A | 5 | a0001c0001t0001g0122 a0001c0001t0001g0188 a0001c0001t0001g0200 others(2): Show |
5 | HG02135.hp1 NA18993.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+2706C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600168 | |||||||
| chr6:106600285 | G | C | 13 | a0001c0003t0002g0012 a0001c0003t0002g0021 a0001c0003t0002g0046 others(10): Show |
14 | HG02135.hp2 HG02148.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.669+2589C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600285 | |||||||
| chr6:106600286 | T | G | 311 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(308): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.669+2588A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600286 | |||||||
| chr6:106600609 | T | G | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.669+2265A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600609 | |||||||
| chr6:106600618 | TTC | T | 5 | a0001c0001t0001g0128 a0001c0001t0001g0212 a0001c0001t0001g0213 others(2): Show |
5 | HG02056.hp2 HG02083.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+2254_669+2255d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600618 | |||||||
| chr6:106600681 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.669+2193C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600681 | |||||||
| chr6:106600737 | G | A | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.669+2137C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600737 | |||||||
| chr6:106600774 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.669+2100A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600774 | |||||||
| chr6:106600834 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.669+2040G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600834 | |||||||
| chr6:106600840 | C | T | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+2034G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600840 | |||||||
| chr6:106600883 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.669+1991C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600883 | |||||||
| chr6:106600918 | A | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+1956T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600918 | |||||||
| chr6:106600937 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.669+1937C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600937 | |||||||
| chr6:106600968 | C | T | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.669+1906G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600968 | |||||||
| chr6:106601008 | A | G | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.669+1866T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601008 | |||||||
| chr6:106601049 | C | T | 7 | a0001c0003t0002g0013 a0001c0003t0002g0101 a0001c0003t0002g0102 others(4): Show |
8 | HG01891.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.669+1825G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601049 | |||||||
| chr6:106601222 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.669+1652C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601222 | |||||||
| chr6:106601307 | G | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1567C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601307 | |||||||
| chr6:106601308 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1566C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601308 | |||||||
| chr6:106601310 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1564A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601310 | |||||||
| chr6:106601312 | C | G | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1562G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601312 | |||||||
| chr6:106601313 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1561A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601313 | |||||||
| chr6:106601318 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1556A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601318 | |||||||
| chr6:106601319 | C | T | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1555G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601319 | |||||||
| chr6:106601331 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1543A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601331 | |||||||
| chr6:106601332 | G | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1542C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601332 | |||||||
| chr6:106601334 | T | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1540A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601334 | |||||||
| chr6:106601338 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1536C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601338 | |||||||
| chr6:106601342 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1532A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601342 | |||||||
| chr6:106601345 | T | G | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1529A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601345 | |||||||
| chr6:106601346 | T | C | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1528A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601346 | |||||||
| chr6:106601349 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1525A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601349 | |||||||
| chr6:106601352 | C | T | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1522G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601352 | |||||||
| chr6:106601356 | C | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1518G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601356 | |||||||
| chr6:106601358 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1516C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601358 | |||||||
| chr6:106601361 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1513C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601361 | |||||||
| chr6:106601362 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1512C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601362 | |||||||
| chr6:106601363 | T | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1511A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601363 | |||||||
| chr6:106601401 | A | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+1473T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601401 | |||||||
| chr6:106601468 | A | C | 1 | a0001c0002t0001g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669+1406T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601468 | |||||||
| chr6:106601491 | T | A | 23 | a0001c0001t0001g0115 a0001c0001t0001g0156 a0001c0001t0001g0161 others(20): Show |
25 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.669+1383A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601491 | |||||||
| chr6:106601641 | G | T | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(311): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.669+1233C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601641 | |||||||
| chr6:106601672 | G | A | 60 | a0001c0001t0001g0115 a0001c0001t0001g0156 a0001c0001t0001g0161 others(57): Show |
69 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.669+1202C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601672 | |||||||
| chr6:106601684 | T | C | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(311): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.669+1190A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601684 | |||||||
| chr6:106601692 | C | G | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+1182G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601692 | |||||||
| chr6:106601739 | T | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+1135A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601739 | |||||||
| chr6:106601783 | G | GT | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+1090dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601783 | |||||||
| chr6:106601814 | T | A | 2 | a0001c0004t0003g0347 a0001c0004t0003g0350 |
2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.669+1060A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601814 | |||||||
| chr6:106602061 | T | C | 2 | a0001c0001t0001g0130 a0001c0002t0001g0108 |
2 | HG02257.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.669+813A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602061 | |||||||
| chr6:106602076 | T | G | 1 | a0001c0005t0008g0355 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+798A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602076 | |||||||
| chr6:106602277 | C | CA | 5 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+596dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602277 | |||||||
| chr6:106602288 | C | G | 1 | a0001c0002t0001g0043 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.669+586G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602288 | |||||||
| chr6:106602309 | T | C | 1 | a0001c0002t0004g0276 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.669+565A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602309 | |||||||
| chr6:106602315 | G | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+559C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602315 | |||||||
| chr6:106602600 | C | T | 1 | a0001c0003t0002g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.669+274G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602600 | |||||||
| chr6:106602621 | A | G | 1 | a0001c0003t0002g0104 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.669+253T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602621 | |||||||
| chr6:106602826 | T | G | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+48A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602826 | |||||||
| chr6:106602857 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.669+17A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602857 | |||||||
| chr6:106602982 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0221 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.621-60C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106602982 | |||||||
| chr6:106602992 | A | T | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(311): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.621-70T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106602992 | |||||||
| chr6:106603071 | G | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0230 a0001c0001t0001g0231 |
3 | HG02109.hp2 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.621-149C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603071 | |||||||
| chr6:106603135 | T | C | 1 | a0001c0001t0005g0361 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.621-213A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603135 | |||||||
| chr6:106603148 | T | A | 1 | a0001c0001t0001g0264 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.621-226A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603148 | |||||||
| chr6:106603156 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02572.hp2 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.621-234G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603156 | |||||||
| chr6:106603265 | G | C | 1 | a0001c0002t0001g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.621-343C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603265 | |||||||
| chr6:106603344 | C | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(200): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.621-422G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603344 | |||||||
| chr6:106603482 | C | T | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.621-560G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603482 | |||||||
| chr6:106603572 | G | A | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621-650C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603572 | |||||||
| chr6:106603621 | C | A | 1 | a0001c0001t0001g0220 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.621-699G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603621 | |||||||
| chr6:106603632 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.621-710T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603632 | |||||||
| chr6:106603680 | T | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-758A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603680 | |||||||
| chr6:106603710 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.621-788A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603710 | |||||||
| chr6:106603897 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.621-975C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603897 | |||||||
| chr6:106604091 | C | A | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.621-1169G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604091 | |||||||
| chr6:106604185 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.621-1263G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604185 | |||||||
| chr6:106604198 | A | G | 7 | a0001c0003t0002g0013 a0001c0003t0002g0101 a0001c0003t0002g0102 others(4): Show |
8 | HG01891.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.621-1276T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604198 | |||||||
| chr6:106604209 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG02165.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.621-1287G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604209 | |||||||
| chr6:106604224 | A | G | 1 | a0001c0003t0002g0097 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.621-1302T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604224 | |||||||
| chr6:106604351 | C | T | 1 | a0001c0003t0002g0045 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.621-1429G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604351 | |||||||
| chr6:106604404 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.621-1482G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604404 | |||||||
| chr6:106604427 | T | G | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.621-1505A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604427 | |||||||
| chr6:106604450 | A | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(200): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.621-1528T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604450 | |||||||
| chr6:106604454 | A | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.621-1532T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604454 | |||||||
| chr6:106604505 | C | T | 1 | a0001c0003t0006g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.621-1583G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604505 | |||||||
| chr6:106604579 | T | C | 1 | a0001c0002t0004g0302 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.621-1657A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604579 | |||||||
| chr6:106604630 | A | G | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.621-1708T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604630 | |||||||
| chr6:106604665 | A | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-1743T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604665 | |||||||
| chr6:106604677 | T | G | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-1755A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604677 | |||||||
| chr6:106604686 | T | A | 1 | a0001c0004t0003g0347 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.621-1764A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604686 | |||||||
| chr6:106604760 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.621-1838T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604760 | |||||||
| chr6:106604851 | T | C | 1 | a0001c0002t0004g0282 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.621-1929A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604851 | |||||||
| chr6:106605161 | C | T | 3 | a0001c0003t0002g0084 a0001c0003t0002g0085 a0001c0003t0002g0087 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.621-2239G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605161 | |||||||
| chr6:106605424 | C | CA | 42 | a0001c0001t0001g0117 a0001c0001t0001g0131 a0001c0001t0001g0171 others(39): Show |
49 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.621-2503dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605424 | |||||||
| chr6:106605446 | A | G | 6 | a0001c0001t0001g0177 a0001c0001t0001g0238 a0001c0001t0001g0239 others(3): Show |
6 | HG00639.hp1 HG00738.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-2524T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605446 | |||||||
| chr6:106605496 | T | C | 2 | a0001c0003t0002g0091 a0001c0003t0002g0096 |
2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.621-2574A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605496 | |||||||
| chr6:106605571 | T | C | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621-2649A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605571 | |||||||
| chr6:106605609 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.621-2687G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605609 | |||||||
| chr6:106605671 | G | T | 2 | a0001c0001t0010g0014 a0001c0001t0010g0116 |
3 | HG02109.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.621-2749C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605671 | |||||||
| chr6:106605731 | A | G | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(248): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.621-2809T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605731 | |||||||
| chr6:106605741 | C | T | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.621-2819G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605741 | |||||||
| chr6:106605752 | G | A | 1 | a0001c0003t0002g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.621-2830C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605752 | |||||||
| chr6:106605773 | C | T | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-2851G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605773 | |||||||
| chr6:106605813 | T | TCA | 16 | a0001c0003t0002g0034 a0001c0003t0002g0037 a0001c0003t0002g0045 others(13): Show |
16 | HG01106.hp2 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.621-2892_621-2891i others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605813 | |||||||
| chr6:106605814 | C | CA | 22 | a0001c0001t0001g0120 a0001c0002t0004g0001 a0001c0002t0004g0017 others(19): Show |
27 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.621-2893_621-2892i others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | |||||||
| chr6:106605814 | CCCAAAA | C | 8 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(5): Show |
9 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.621-2898_621-2893d others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | |||||||
| chr6:106605814 | CCCAAAAA | C | 37 | a0001c0001t0001g0184 a0001c0004t0003g0002 a0001c0004t0003g0005 others(34): Show |
44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.621-2899_621-2893d others(9): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | |||||||
| chr6:106605814 | CCCAAAAA others(2): Show |
C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0144 a0001c0001t0001g0158 others(1): Show |
4 | HG00140.hp2 HG02738.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.621-2901_621-2893d others(11): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | |||||||
| chr6:106605814 | CCCAAAAA others(3): Show |
C | 55 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0135 others(52): Show |
55 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.621-2902_621-2893d others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | |||||||
| chr6:106605814 | CCCAAAAA others(4): Show |
C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(151): Show |
163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.621-2903_621-2893d others(13): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | |||||||
| chr6:106605814 | CCCAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.621-2904_621-2893d others(14): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | |||||||
| chr6:106605815 | C | A | 82 | a0001c0001t0001g0015 a0001c0001t0001g0152 a0001c0002t0004g0016 others(79): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.621-2893G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605815 | |||||||
| chr6:106605816 | C | A | 23 | a0001c0001t0001g0120 a0001c0002t0004g0001 a0001c0002t0004g0017 others(20): Show |
28 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.621-2894G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605816 | |||||||
| chr6:106605816 | C | CAA | 12 | a0001c0002t0004g0016 a0001c0002t0004g0018 a0001c0002t0004g0276 others(9): Show |
13 | HG00408.hp1 HG00423.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.621-2896_621-2895d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605816 | |||||||
| chr6:106605817 | A | AC | 42 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(39): Show |
45 | HG00280.hp2 HG00639.hp2 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.621-2896_621-2895i others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605817 | |||||||
| chr6:106605818 | A | C | 3 | a0001c0003t0002g0050 a0001c0003t0013g0109 a0003c0012t0001g0275 |
3 | HG03209.hp2 NA18747.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.621-2896T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605818 | |||||||
| chr6:106605822 | A | C | 8 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(5): Show |
9 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.621-2900T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605822 | |||||||
| chr6:106605823 | A | C | 37 | a0001c0001t0001g0184 a0001c0004t0003g0002 a0001c0004t0003g0005 others(34): Show |
44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.621-2901T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605823 | |||||||
| chr6:106605825 | A | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0144 a0001c0001t0001g0158 others(1): Show |
4 | HG00140.hp2 HG02738.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.621-2903T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605825 | |||||||
| chr6:106605826 | A | C | 55 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0135 others(52): Show |
55 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.621-2904T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605826 | |||||||
| chr6:106605827 | A | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(151): Show |
163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.621-2905T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605827 | |||||||
| chr6:106605828 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.621-2906T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605828 | |||||||
| chr6:106605884 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.621-2962T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605884 | |||||||
| chr6:106605895 | G | A | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621-2973C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605895 | |||||||
| chr6:106605972 | A | G | 7 | a0001c0003t0002g0013 a0001c0003t0002g0101 a0001c0003t0002g0102 others(4): Show |
8 | HG01891.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.621-3050T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605972 | |||||||
| chr6:106605973 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.621-3051C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605973 | |||||||
| chr6:106606122 | C | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(200): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.621-3200G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606122 | |||||||
| chr6:106606228 | C | T | 1 | a0001c0011t0002g0112 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.621-3306G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606228 | |||||||
| chr6:106606263 | A | G | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.621-3341T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606263 | |||||||
| chr6:106606292 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | NA18948.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.621-3370C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606292 | |||||||
| chr6:106606351 | C | T | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.621-3429G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606351 | |||||||
| chr6:106606366 | G | C | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.621-3444C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606366 | |||||||
| chr6:106606444 | C | T | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(248): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.621-3522G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606444 | |||||||
| chr6:106606635 | G | A | 2 | a0001c0002t0004g0300 a0001c0003t0002g0095 |
2 | HG01192.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.621-3713C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606635 | |||||||
| chr6:106606867 | A | C | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.621-3945T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606867 | |||||||
| chr6:106606915 | T | G | 1 | a0001c0003t0002g0104 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621-3993A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606915 | |||||||
| chr6:106606961 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(80): Show |
87 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.621-4039A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606961 | |||||||
| chr6:106606972 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621-4050C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606972 | |||||||
| chr6:106606996 | A | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(211): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.621-4074T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606996 | |||||||
| chr6:106607035 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.621-4113T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607035 | |||||||
| chr6:106607036 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0129 a0001c0001t0001g0170 others(7): Show |
12 | HG00438.hp1 HG02071.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.621-4114G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607036 | |||||||
| chr6:106607283 | C | CA | 39 | a0001c0001t0001g0145 a0001c0001t0001g0255 a0001c0002t0004g0001 others(36): Show |
46 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.621-4362dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607283 | |||||||
| chr6:106607486 | T | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.621-4564A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607486 | |||||||
| chr6:106607529 | CA | C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(248): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.621-4608delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607529 | |||||||
| chr6:106607565 | G | T | 1 | a0001c0003t0002g0089 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.621-4643C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607565 | |||||||
| chr6:106607707 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.621-4785G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607707 | |||||||
| chr6:106607721 | T | C | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621-4799A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607721 | |||||||
| chr6:106607815 | T | C | 20 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0033 others(17): Show |
21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.621-4893A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607815 | |||||||
| chr6:106607826 | CA | C | 61 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(58): Show |
64 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.621-4905delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607826 | |||||||
| chr6:106607832 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.621-4910T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607832 | |||||||
| chr6:106607833 | A | G | 61 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(58): Show |
64 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.621-4911T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607833 | |||||||
| chr6:106607865 | G | T | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.621-4943C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607865 | |||||||
| chr6:106607952 | G | A | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(311): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.621-5030C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607952 | |||||||
| chr6:106608031 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621-5109G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608031 | |||||||
| chr6:106608285 | A | C | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.621-5363T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608285 | |||||||
| chr6:106608494 | T | C | 9 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(6): Show |
9 | HG02451.hp1 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-5572A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608494 | |||||||
| chr6:106608526 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(271): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.621-5604A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608526 | |||||||
| chr6:106608622 | C | T | 1 | a0001c0003t0006g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.621-5700G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608622 | |||||||
| chr6:106608651 | T | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-5729A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608651 | |||||||
| chr6:106608783 | G | GA | 8 | a0001c0004t0003g0002 a0001c0004t0003g0324 a0001c0004t0003g0334 others(5): Show |
11 | HG01192.hp1 HG01255.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.621-5862dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608783 | |||||||
| chr6:106609097 | C | T | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-6175G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609097 | |||||||
| chr6:106609161 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621-6239A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609161 | |||||||
| chr6:106609305 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.621-6383C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609305 | |||||||
| chr6:106609392 | G | A | 38 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(35): Show |
45 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.621-6470C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609392 | |||||||
| chr6:106609599 | G | A | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.621-6677C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609599 | |||||||
| chr6:106609651 | A | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0186 |
2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.621-6729T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609651 | |||||||
| chr6:106609680 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.621-6758A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609680 | |||||||
| chr6:106609716 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.621-6794G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609716 | |||||||
| chr6:106609869 | C | A | 1 | a0001c0003t0002g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.621-6947G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609869 | |||||||
| chr6:106609900 | A | AC | 6 | a0001c0003t0002g0061 a0001c0003t0002g0091 a0001c0003t0002g0093 others(3): Show |
6 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-6979dupG | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609900 | |||||||
| chr6:106609906 | A | T | 1 | a0001c0002t0004g0285 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.621-6984T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609906 | |||||||
| chr6:106609973 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0180 |
2 | HG00558.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.621-7051T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609973 | |||||||
| chr6:106609980 | G | A | 1 | a0001c0005t0008g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.621-7058C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609980 | |||||||
| chr6:106610067 | AT | A | 65 | a0001c0001t0001g0176 a0001c0002t0009g0305 a0001c0002t0009g0306 others(62): Show |
68 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.621-7146delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610067 | |||||||
| chr6:106610101 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.621-7179C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610101 | |||||||
| chr6:106610342 | G | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-7420C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610342 | |||||||
| chr6:106610362 | C | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(212): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.621-7440G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610362 | |||||||
| chr6:106610394 | C | A | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.621-7472G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610394 | |||||||
| chr6:106610517 | A | C | 55 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0135 others(52): Show |
55 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.621-7595T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610517 | |||||||
| chr6:106610529 | G | C | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621-7607C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610529 | |||||||
| chr6:106610621 | G | A | 35 | a0001c0002t0001g0042 a0001c0002t0001g0076 a0001c0002t0004g0001 others(32): Show |
42 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.621-7699C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610621 | |||||||
| chr6:106610689 | T | TCAAAATC others(314): Show |
2 | a0001c0004t0003g0345 a0001c0004t0003g0346 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.621-7768_621-7767i others(323): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610689 | |||||||
| chr6:106610689 | T | TCAAAATC others(315): Show |
2 | a0001c0004t0003g0343 a0001c0004t0003g0344 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.621-7768_621-7767i others(324): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610689 | |||||||
| chr6:106610702 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621-7780C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610702 | |||||||
| chr6:106610746 | G | C | 1 | a0001c0001t0005g0368 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.621-7824C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610746 | |||||||
| chr6:106610954 | T | G | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621-8032A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610954 | |||||||
| chr6:106610994 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.621-8072C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610994 | |||||||
| chr6:106611035 | C | G | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(200): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.621-8113G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611035 | |||||||
| chr6:106611048 | C | CA | 39 | a0001c0001t0001g0178 a0001c0001t0001g0219 a0001c0001t0005g0361 others(36): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.621-8127dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611048 | |||||||
| chr6:106611060 | C | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-8138G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611060 | |||||||
| chr6:106611168 | G | A | 1 | a0001c0003t0006g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.620+8034C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611168 | |||||||
| chr6:106611178 | G | A | 1 | a0001c0004t0003g0315 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.620+8024C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611178 | |||||||
| chr6:106611278 | T | C | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+7924A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611278 | |||||||
| chr6:106611346 | T | C | 3 | a0001c0004t0003g0351 a0001c0004t0003g0352 a0001c0004t0003g0353 |
3 | HG01192.hp1 HG01255.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.620+7856A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611346 | |||||||
| chr6:106611387 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.620+7815C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611387 | |||||||
| chr6:106611582 | T | C | 38 | a0001c0001t0001g0171 a0001c0002t0004g0001 a0001c0002t0004g0016 others(35): Show |
45 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.620+7620A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611582 | |||||||
| chr6:106611596 | C | G | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+7606G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611596 | |||||||
| chr6:106611596 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(80): Show |
87 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.620+7606G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611596 | |||||||
| chr6:106611735 | C | T | 1 | a0001c0004t0003g0351 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.620+7467G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611735 | |||||||
| chr6:106611779 | T | A | 1 | a0001c0002t0001g0062 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.620+7423A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611779 | |||||||
| chr6:106612008 | G | C | 60 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(57): Show |
63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.620+7194C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612008 | |||||||
| chr6:106612016 | C | A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+7186G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612016 | |||||||
| chr6:106612088 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.620+7114C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612088 | |||||||
| chr6:106612112 | C | T | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+7090G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612112 | |||||||
| chr6:106612184 | C | T | 1 | a0004c0007t0001g0081 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.620+7018G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612184 | |||||||
| chr6:106612211 | A | AC | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+6990dupG | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612211 | |||||||
| chr6:106612272 | A | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+6930T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612272 | |||||||
| chr6:106612279 | C | T | 1 | a0001c0003t0002g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.620+6923G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612279 | |||||||
| chr6:106612384 | C | CA | 69 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0001g0118 others(66): Show |
71 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.620+6817dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | |||||||
| chr6:106612384 | C | CAA | 7 | a0001c0001t0001g0115 a0001c0001t0001g0185 a0001c0001t0001g0271 others(4): Show |
7 | HG01517.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+6816_620+6817d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | |||||||
| chr6:106612384 | CA | C | 53 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0182 others(50): Show |
62 | HG00544.hp2 HG00597.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.620+6817delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | |||||||
| chr6:106612384 | CAA | C | 21 | a0001c0002t0001g0008 a0001c0003t0002g0009 a0001c0003t0002g0033 others(18): Show |
23 | HG00280.hp2 HG02074.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.620+6816_620+6817d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | |||||||
| chr6:106612384 | CAAAAAAA others(10): Show |
C | 4 | a0001c0004t0003g0343 a0001c0004t0003g0344 a0001c0004t0003g0345 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+6801_620+6817d others(19): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | |||||||
| chr6:106612480 | G | A | 1 | a0001c0003t0002g0061 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.620+6722C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612480 | |||||||
| chr6:106612559 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(85): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.620+6643G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612559 | |||||||
| chr6:106612560 | G | A | 1 | a0001c0004t0003g0338 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.620+6642C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612560 | |||||||
| chr6:106612563 | T | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0128 a0001c0001t0001g0129 others(14): Show |
19 | HG00438.hp1 HG02056.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.620+6639A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612563 | |||||||
| chr6:106612655 | T | TACCTACT others(21): Show |
314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(311): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.620+6546_620+6547i others(30): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612655 | |||||||
| chr6:106612855 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+6347C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612855 | |||||||
| chr6:106612864 | G | A | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(200): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.620+6338C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612864 | |||||||
| chr6:106612892 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0172 |
2 | NA18991.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.620+6310T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612892 | |||||||
| chr6:106612933 | T | A | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+6269A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612933 | |||||||
| chr6:106612961 | T | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(211): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.620+6241A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612961 | |||||||
| chr6:106613013 | C | T | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+6189G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613013 | |||||||
| chr6:106613257 | C | T | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+5945G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613257 | |||||||
| chr6:106613387 | G | A | 6 | a0001c0004t0003g0006 a0001c0004t0003g0019 a0001c0004t0003g0339 others(3): Show |
9 | HG02056.hp1 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.620+5815C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613387 | |||||||
| chr6:106613455 | C | T | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+5747G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613455 | |||||||
| chr6:106613569 | A | C | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+5633T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613569 | |||||||
| chr6:106613677 | T | G | 1 | a0001c0003t0006g0030 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.620+5525A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613677 | |||||||
| chr6:106613756 | A | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+5446T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613756 | |||||||
| chr6:106613783 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.620+5419C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613783 | |||||||
| chr6:106614081 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.620+5121C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614081 | |||||||
| chr6:106614312 | T | C | 37 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(34): Show |
44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+4890A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614312 | |||||||
| chr6:106614357 | T | C | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+4845A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614357 | |||||||
| chr6:106614454 | T | C | 1 | a0001c0002t0001g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.620+4748A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614454 | |||||||
| chr6:106614482 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.620+4720C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614482 | |||||||
| chr6:106614487 | A | C | 1 | a0001c0001t0005g0361 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.620+4715T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614487 | |||||||
| chr6:106614543 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0221 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.620+4659G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614543 | |||||||
| chr6:106614600 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.620+4602G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614600 | |||||||
| chr6:106614609 | G | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(200): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.620+4593C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614609 | |||||||
| chr6:106614853 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | NA18948.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.620+4349A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614853 | |||||||
| chr6:106614883 | C | T | 1 | a0001c0004t0003g0323 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.620+4319G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614883 | |||||||
| chr6:106614952 | A | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(271): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.620+4250T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614952 | |||||||
| chr6:106614952 | A | T | 1 | a0001c0001t0001g0226 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.620+4250T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614952 | |||||||
| chr6:106614959 | A | AC | 13 | a0001c0001t0001g0123 a0001c0001t0001g0131 a0001c0001t0001g0132 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.620+4242dupG | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614959 | |||||||
| chr6:106614959 | A | C | 1 | a0001c0011t0002g0112 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.620+4243T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614959 | |||||||
| chr6:106614965 | C | G | 2 | a0001c0003t0002g0057 a0001c0003t0002g0088 |
2 | NA18966.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.620+4237G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614965 | |||||||
| chr6:106615006 | G | C | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+4196C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615006 | |||||||
| chr6:106615014 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.620+4188A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615014 | |||||||
| chr6:106615127 | C | A | 8 | a0001c0003t0002g0013 a0001c0003t0002g0101 a0001c0003t0002g0102 others(5): Show |
9 | HG01891.hp1 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.620+4075G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615127 | |||||||
| chr6:106615216 | G | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+3986C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615216 | |||||||
| chr6:106615287 | C | T | 190 | a0001c0001t0001g0115 a0001c0001t0001g0130 a0001c0001t0001g0135 others(187): Show |
198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.620+3915G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615287 | |||||||
| chr6:106615344 | A | G | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.620+3858T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615344 | |||||||
| chr6:106615408 | C | CA | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+3793dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615408 | |||||||
| chr6:106615544 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(217): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.620+3658T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615544 | |||||||
| chr6:106615568 | G | A | 2 | a0001c0002t0001g0042 a0001c0008t0001g0032 |
2 | HG01516.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.620+3634C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615568 | |||||||
| chr6:106615665 | A | G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(205): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.620+3537T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615665 | |||||||
| chr6:106615683 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(204): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.620+3519C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615683 | |||||||
| chr6:106615783 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(204): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.620+3419G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615783 | |||||||
| chr6:106615784 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(204): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.620+3418C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615784 | |||||||
| chr6:106615856 | C | T | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+3346G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615856 | |||||||
| chr6:106615886 | T | C | 30 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0021 others(27): Show |
32 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.620+3316A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615886 | |||||||
| chr6:106616006 | A | G | 1 | a0001c0004t0003g0321 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.620+3196T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616006 | |||||||
| chr6:106616007 | C | T | 33 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(30): Show |
41 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.620+3195G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616007 | |||||||
| chr6:106616025 | C | T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(172): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.620+3177G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616025 | |||||||
| chr6:106616046 | G | A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+3156C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616046 | |||||||
| chr6:106616076 | G | A | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+3126C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616076 | |||||||
| chr6:106616277 | A | C | 1 | a0001c0003t0002g0022 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.620+2925T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616277 | |||||||
| chr6:106616345 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.620+2857C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616345 | |||||||
| chr6:106616360 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.620+2842A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616360 | |||||||
| chr6:106616566 | CAATAGCT | C | 123 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(120): Show |
136 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.620+2629_620+2635d others(9): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616566 | |||||||
| chr6:106616576 | T | C | 122 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(119): Show |
135 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.620+2626A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616576 | |||||||
| chr6:106616713 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.620+2489A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616713 | |||||||
| chr6:106616790 | G | A | 2 | a0001c0008t0001g0032 a0003c0012t0001g0275 |
2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.620+2412C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616790 | |||||||
| chr6:106616936 | C | A | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+2266G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616936 | |||||||
| chr6:106616970 | G | A | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+2232C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616970 | |||||||
| chr6:106616981 | G | A | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+2221C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616981 | |||||||
| chr6:106617013 | A | AAG | 22 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(19): Show |
25 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.620+2187_620+2188d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617013 | |||||||
| chr6:106617054 | T | C | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+2148A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617054 | |||||||
| chr6:106617202 | T | A | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+2000A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617202 | |||||||
| chr6:106617225 | A | G | 54 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(51): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.620+1977T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617225 | |||||||
| chr6:106617239 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.620+1963T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617239 | |||||||
| chr6:106617252 | C | T | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+1950G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617252 | |||||||
| chr6:106617331 | G | C | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+1871C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617331 | |||||||
| chr6:106617404 | C | T | 54 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(51): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.620+1798G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617404 | |||||||
| chr6:106617405 | A | T | 1 | a0001c0001t0005g0361 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.620+1797T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617405 | |||||||
| chr6:106617411 | T | C | 2 | a0001c0003t0002g0050 a0001c0011t0002g0112 |
2 | NA18747.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.620+1791A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617411 | |||||||
| chr6:106617463 | C | A | 2 | a0001c0008t0001g0032 a0003c0012t0001g0275 |
2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.620+1739G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617463 | |||||||
| chr6:106617501 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.620+1701G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617501 | |||||||
| chr6:106617604 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+1598C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617604 | |||||||
| chr6:106617638 | G | A | 54 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(51): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.620+1564C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617638 | |||||||
| chr6:106617738 | C | T | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+1464G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617738 | |||||||
| chr6:106617758 | C | A | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+1444G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617758 | |||||||
| chr6:106617947 | A | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+1255T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617947 | |||||||
| chr6:106618111 | A | G | 1 | a0001c0002t0004g0283 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.620+1091T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618111 | |||||||
| chr6:106618115 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.620+1087G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618115 | |||||||
| chr6:106618127 | T | A | 56 | a0001c0002t0001g0008 a0001c0003t0013g0109 a0001c0004t0003g0002 others(53): Show |
65 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.620+1075A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618127 | |||||||
| chr6:106618133 | T | C | 97 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(94): Show |
103 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.620+1069A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618133 | |||||||
| chr6:106618137 | A | G | 97 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(94): Show |
103 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.620+1065T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618137 | |||||||
| chr6:106618227 | CA | C | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+974delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618227 | |||||||
| chr6:106618282 | T | TA | 55 | a0001c0002t0001g0008 a0001c0004t0003g0002 a0001c0004t0003g0005 others(52): Show |
64 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.620+919dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618282 | |||||||
| chr6:106618282 | TA | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(83): Show |
90 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.620+919delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618282 | |||||||
| chr6:106618295 | GTTATT | G | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+902_620+906del others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618295 | |||||||
| chr6:106618443 | C | T | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+759G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618443 | |||||||
| chr6:106618580 | A | G | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+622T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618580 | |||||||
| chr6:106618594 | G | A | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.620+608C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618594 | |||||||
| chr6:106618618 | A | C | 130 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(127): Show |
143 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.620+584T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618618 | |||||||
| chr6:106618624 | G | A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+578C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618624 | |||||||
| chr6:106618668 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0271 |
2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.620+534C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618668 | |||||||
| chr6:106618668 | G | T | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+534C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618668 | |||||||
| chr6:106618678 | T | C | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+524A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618678 | |||||||
| chr6:106618797 | G | A | 4 | a0001c0003t0002g0051 a0001c0003t0002g0052 a0001c0003t0002g0053 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+405C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618797 | |||||||
| chr6:106618863 | C | CT | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+338dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618863 | |||||||
| chr6:106618893 | T | C | 3 | a0001c0004t0003g0351 a0001c0004t0003g0352 a0001c0004t0003g0353 |
3 | HG01192.hp1 HG01255.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.620+309A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618893 | |||||||
| chr6:106619006 | G | A | 52 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(49): Show |
60 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.620+196C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106619006 | |||||||
| chr6:106619023 | T | C | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+179A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106619023 | |||||||
| chr6:106619098 | C | T | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+104G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106619098 | |||||||
| chr6:106619124 | C | A | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.620+78G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106619124 | |||||||
| chr6:106619544 | CACA | C | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.496-221_496-219del others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619544 | |||||||
| chr6:106619570 | T | A | 88 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(85): Show |
94 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.496-244A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619570 | |||||||
| chr6:106619589 | T | TA | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-264dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619589 | |||||||
| chr6:106619595 | T | A | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-269A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619595 | |||||||
| chr6:106619606 | A | AT | 43 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0162 others(40): Show |
45 | HG00280.hp2 HG00597.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.496-281dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619606 | |||||||
| chr6:106619606 | AT | A | 47 | a0001c0001t0001g0131 a0001c0001t0001g0165 a0001c0001t0001g0221 others(44): Show |
50 | HG00438.hp2 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.496-281delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619606 | |||||||
| chr6:106619606 | ATT | A | 33 | a0001c0002t0001g0042 a0001c0002t0004g0001 a0001c0002t0004g0016 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.496-282_496-281del others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619606 | |||||||
| chr6:106619606 | ATTTT | A | 50 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(47): Show |
58 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.496-284_496-281del others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619606 | |||||||
| chr6:106619634 | C | T | 1 | a0001c0003t0002g0034 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.496-308G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619634 | |||||||
| chr6:106619635 | G | A | 1 | a0003c0012t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.496-309C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619635 | |||||||
| chr6:106619684 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0267 |
2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.496-358A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619684 | |||||||
| chr6:106619701 | T | C | 1 | a0001c0004t0003g0356 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.496-375A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619701 | |||||||
| chr6:106619705 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.496-379C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619705 | |||||||
| chr6:106619776 | T | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.496-450A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619776 | |||||||
| chr6:106619778 | AT | A | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-453delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619778 | |||||||
| chr6:106619813 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.496-487C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619813 | |||||||
| chr6:106619847 | G | A | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-521C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619847 | |||||||
| chr6:106619857 | C | T | 130 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(127): Show |
143 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.496-531G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619857 | |||||||
| chr6:106619890 | C | T | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-564G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619890 | |||||||
| chr6:106619921 | TTAA | T | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-598_496-596del others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619921 | |||||||
| chr6:106619951 | G | T | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-625C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619951 | |||||||
| chr6:106619976 | T | G | 1 | a0001c0004t0003g0354 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.496-650A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619976 | |||||||
| chr6:106620070 | T | A | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-744A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620070 | |||||||
| chr6:106620255 | A | C | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-929T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620255 | |||||||
| chr6:106620357 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496-1031G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620357 | |||||||
| chr6:106620518 | C | T | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.495+907G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620518 | |||||||
| chr6:106620558 | C | T | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.495+867G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620558 | |||||||
| chr6:106620716 | A | G | 2 | a0001c0001t0005g0358 a0001c0001t0005g0359 |
2 | HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.495+709T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620716 | |||||||
| chr6:106620776 | A | G | 1 | a0001c0003t0006g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.495+649T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620776 | |||||||
| chr6:106620826 | G | A | 8 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG01099.hp1 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+599C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620826 | |||||||
| chr6:106620904 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0230 a0001c0001t0001g0231 |
3 | HG02109.hp2 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.495+521G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620904 | |||||||
| chr6:106621071 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.495+354C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621071 | |||||||
| chr6:106621182 | CA | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(82): Show |
89 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.495+242delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621182 | |||||||
| chr6:106621234 | C | G | 20 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0033 others(17): Show |
21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.495+191G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621234 | |||||||
| chr6:106621265 | A | G | 3 | a0001c0005t0008g0310 a0001c0005t0008g0311 a0001c0005t0008g0318 |
3 | HG02615.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.495+160T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621265 | |||||||
| chr6:106621357 | G | A | 363 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(360): Show |
390 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.495+68C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621357 | |||||||
| chr6:106621383 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.495+42C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621383 | |||||||
| chr6:106621398 | T | C | 186 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0010 others(183): Show |
208 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.495+27A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621398 | |||||||
| chr6:106621535 | T | C | 20 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0033 others(17): Show |
21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.427-42A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621535 | |||||||
| chr6:106621547 | G | A | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.427-54C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621547 | |||||||
| chr6:106621576 | T | G | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-83A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621576 | |||||||
| chr6:106621744 | A | G | 2 | a0001c0004t0003g0313 a0001c0004t0003g0314 |
2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.427-251T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621744 | |||||||
| chr6:106621843 | C | T | 1 | a0001c0002t0001g0043 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.427-350G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621843 | |||||||
| chr6:106622017 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.427-524A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622017 | |||||||
| chr6:106622074 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.427-581A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622074 | |||||||
| chr6:106622104 | AAC | A | 20 | a0001c0003t0002g0012 a0001c0003t0002g0021 a0001c0003t0002g0046 others(17): Show |
21 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.427-613_427-612del others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622104 | |||||||
| chr6:106622168 | CA | C | 52 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(49): Show |
60 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.426+649delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622168 | |||||||
| chr6:106622286 | T | C | 2 | a0001c0003t0013g0109 a0003c0012t0001g0275 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.426+532A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622286 | |||||||
| chr6:106622354 | T | A | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.426+464A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622354 | |||||||
| chr6:106622576 | G | A | 52 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(49): Show |
60 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.426+242C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622576 | |||||||
| chr6:106622639 | G | T | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.426+179C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622639 | |||||||
| chr6:106622653 | C | T | 52 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(49): Show |
60 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.426+165G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622653 | |||||||
| chr6:106622745 | C | T | 2 | a0001c0001t0001g0177 a0001c0008t0001g0032 |
2 | HG01934.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.426+73G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622745 | |||||||
| chr6:106622790 | G | A | 2 | a0001c0001t0001g0266 a0001c0002t0001g0008 |
3 | HG00738.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.426+28C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622790 | |||||||
| chr6:106623051 | A | G | 33 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(30): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.275-82T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623051 | |||||||
| chr6:106623093 | C | A | 21 | a0001c0003t0002g0012 a0001c0003t0002g0021 a0001c0003t0002g0046 others(18): Show |
22 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.275-124G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623093 | |||||||
| chr6:106623149 | ACT | A | 22 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(19): Show |
25 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.275-182_275-181del others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623149 | |||||||
| chr6:106623239 | G | A | 2 | a0001c0001t0010g0014 a0001c0001t0010g0116 |
3 | HG02109.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.275-270C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623239 | |||||||
| chr6:106623309 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.275-340T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623309 | |||||||
| chr6:106623326 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.275-357C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623326 | |||||||
| chr6:106623424 | T | C | 1 | a0001c0003t0002g0022 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.275-455A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623424 | |||||||
| chr6:106623434 | G | A | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.275-465C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623434 | |||||||
| chr6:106623472 | G | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-503C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623472 | |||||||
| chr6:106623545 | A | T | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-576T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623545 | |||||||
| chr6:106623601 | T | A | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.275-632A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623601 | |||||||
| chr6:106623616 | T | C | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.275-647A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623616 | |||||||
| chr6:106623720 | T | A | 1 | a0001c0003t0002g0045 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.275-751A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623720 | |||||||
| chr6:106623760 | T | C | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-791A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623760 | |||||||
| chr6:106623767 | G | A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-798C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623767 | |||||||
| chr6:106623798 | C | T | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-829G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623798 | |||||||
| chr6:106623799 | A | G | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-830T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623799 | |||||||
| chr6:106623872 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.275-903A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623872 | |||||||
| chr6:106623901 | G | C | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.275-932C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623901 | |||||||
| chr6:106623920 | C | A | 190 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0010 others(187): Show |
212 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.275-951G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623920 | |||||||
| chr6:106623967 | T | C | 2 | a0001c0003t0002g0053 a0001c0003t0002g0054 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.275-998A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623967 | |||||||
| chr6:106624003 | G | T | 1 | a0001c0002t0001g0062 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.275-1034C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624003 | |||||||
| chr6:106624061 | T | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-1092A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624061 | |||||||
| chr6:106624211 | A | G | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.275-1242T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624211 | |||||||
| chr6:106624244 | T | C | 190 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0010 others(187): Show |
212 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.275-1275A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624244 | |||||||
| chr6:106624245 | G | C | 53 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(50): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.275-1276C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624245 | |||||||
| chr6:106624259 | T | A | 1 | a0005c0010t0002g0110 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.275-1290A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624259 | |||||||
| chr6:106624284 | T | G | 190 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0010 others(187): Show |
212 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.275-1315A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624284 | |||||||
| chr6:106624289 | C | T | 1 | a0001c0003t0002g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.275-1320G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624289 | |||||||
| chr6:106624297 | G | A | 1 | a0001c0003t0002g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.275-1328C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624297 | |||||||
| chr6:106624300 | C | T | 20 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0033 others(17): Show |
21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.275-1331G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624300 | |||||||
| chr6:106624349 | C | T | 20 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0033 others(17): Show |
21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.275-1380G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624349 | |||||||
| chr6:106624398 | C | T | 1 | a0001c0002t0004g0276 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.275-1429G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624398 | |||||||
| chr6:106624401 | A | G | 342 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0111 others(339): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.275-1432T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624401 | |||||||
| chr6:106624499 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-1530C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624499 | |||||||
| chr6:106624538 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.275-1569A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624538 | |||||||
| chr6:106624575 | G | A | 2 | a0001c0003t0013g0109 a0003c0012t0001g0275 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.275-1606C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624575 | |||||||
| chr6:106624616 | G | A | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-1647C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624616 | |||||||
| chr6:106624746 | A | C | 1 | a0001c0004t0003g0317 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.275-1777T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624746 | |||||||
| chr6:106624756 | T | C | 1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.275-1787A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624756 | |||||||
| chr6:106624839 | G | A | 1 | a0001c0005t0008g0355 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.275-1870C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624839 | |||||||
| chr6:106624898 | T | A | 1 | a0005c0010t0002g0110 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.275-1929A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624898 | |||||||
| chr6:106624935 | C | CA | 16 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0173 others(13): Show |
17 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.275-1967dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624935 | |||||||
| chr6:106624936 | A | G | 1 | a0001c0002t0009g0308 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.275-1967T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624936 | |||||||
| chr6:106624942 | AAAAAAAA others(3): Show |
A | 4 | a0001c0002t0009g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-1983_275-1974d others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624942 | |||||||
| chr6:106624946 | A | AAAAAAG | 32 | a0001c0002t0004g0001 a0001c0002t0004g0016 a0001c0002t0004g0017 others(29): Show |
39 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.275-1983_275-1978d others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624946 | |||||||
| chr6:106624946 | A | AAAAAAGA others(5): Show |
1 | a0001c0002t0004g0278 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.275-1989_275-1978d others(14): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624946 | |||||||
| chr6:106624946 | AAAAAAG | A | 59 | a0001c0003t0002g0009 a0001c0003t0002g0022 a0001c0003t0002g0033 others(56): Show |
68 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.275-1983_275-1978d others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624946 | |||||||
| chr6:106624946 | AAAAAAGA others(5): Show |
A | 3 | a0001c0001t0001g0144 a0001c0003t0002g0095 a0001c0003t0002g0100 |
3 | HG01192.hp2 HG02055.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.275-1989_275-1978d others(14): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624946 | |||||||
| chr6:106624947 | AAAAAG | A | 14 | a0001c0004t0003g0313 a0001c0004t0003g0314 a0001c0004t0003g0316 others(11): Show |
14 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.275-1983_275-1979d others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624947 | |||||||
| chr6:106625035 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02572.hp2 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.275-2066G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625035 | |||||||
| chr6:106625198 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.275-2229C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625198 | |||||||
| chr6:106625264 | C | A | 1 | a0001c0005t0008g0342 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.275-2295G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625264 | |||||||
| chr6:106625290 | C | T | 1 | a0001c0003t0002g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.275-2321G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625290 | |||||||
| chr6:106625388 | C | T | 3 | a0001c0004t0003g0313 a0001c0004t0003g0314 a0001c0004t0003g0316 |
3 | HG01175.hp1 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.275-2419G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625388 | |||||||
| chr6:106625389 | G | A | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0167 others(4): Show |
7 | HG02258.hp1 HG02717.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-2420C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625389 | |||||||
| chr6:106625524 | T | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-2555A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625524 | |||||||
| chr6:106625535 | A | T | 54 | a0001c0003t0002g0009 a0001c0003t0002g0012 a0001c0003t0002g0013 others(51): Show |
57 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.275-2566T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625535 | |||||||
| chr6:106625614 | G | A | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.275-2645C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625614 | |||||||
| chr6:106625627 | C | T | 1 | a0001c0004t0003g0315 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.275-2658G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625627 | |||||||
| chr6:106625645 | C | T | 2 | a0001c0004t0003g0313 a0001c0004t0003g0314 |
2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.275-2676G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625645 | |||||||
| chr6:106625661 | C | CT | 74 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(71): Show |
85 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.275-2693dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625661 | |||||||
| chr6:106625665 | T | TC | 54 | a0001c0003t0002g0082 a0001c0004t0003g0002 a0001c0004t0003g0005 others(51): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.275-2697_275-2696i others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625665 | |||||||
| chr6:106625732 | C | G | 54 | a0001c0003t0002g0082 a0001c0004t0003g0002 a0001c0004t0003g0005 others(51): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.275-2763G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625732 | |||||||
| chr6:106625750 | G | A | 1 | a0001c0005t0008g0355 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.275-2781C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625750 | |||||||
| chr6:106625813 | G | A | 1 | a0001c0002t0009g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.275-2844C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625813 | |||||||
| chr6:106625868 | A | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+2880T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625868 | |||||||
| chr6:106625908 | G | A | 1 | a0001c0002t0004g0016 | 2 | NA18952.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.274+2840C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625908 | |||||||
| chr6:106625996 | G | A | 2 | a0001c0003t0013g0109 a0003c0012t0001g0275 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.274+2752C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625996 | |||||||
| chr6:106626008 | A | G | 57 | a0001c0003t0002g0082 a0001c0003t0013g0109 a0001c0004t0003g0002 others(54): Show |
65 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.274+2740T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626008 | |||||||
| chr6:106626064 | T | C | 31 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(28): Show |
34 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.274+2684A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626064 | |||||||
| chr6:106626135 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.274+2613G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626135 | |||||||
| chr6:106626161 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.274+2587C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626161 | |||||||
| chr6:106626238 | T | C | 1 | a0001c0003t0002g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.274+2510A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626238 | |||||||
| chr6:106626341 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.274+2407G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626341 | |||||||
| chr6:106626344 | T | C | 1 | a0001c0002t0004g0302 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.274+2404A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626344 | |||||||
| chr6:106626383 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.274+2365T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626383 | |||||||
| chr6:106626591 | C | T | 1 | a0005c0010t0002g0110 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.274+2157G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626591 | |||||||
| chr6:106626592 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.274+2156A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626592 | |||||||
| chr6:106626730 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.274+2018C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626730 | |||||||
| chr6:106626946 | G | A | 55 | a0001c0003t0013g0109 a0001c0004t0003g0002 a0001c0004t0003g0005 others(52): Show |
63 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.274+1802C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626946 | |||||||
| chr6:106626983 | C | A | 1 | a0001c0004t0003g0356 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.274+1765G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626983 | |||||||
| chr6:106627141 | G | GA | 365 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(362): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.274+1606dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627141 | |||||||
| chr6:106627310 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0163 others(2): Show |
7 | NA18952.hp2 NA18978.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.274+1438G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627310 | |||||||
| chr6:106627389 | T | C | 2 | a0001c0004t0003g0356 a0001c0005t0008g0355 |
2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.274+1359A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627389 | |||||||
| chr6:106627574 | A | G | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+1174T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627574 | |||||||
| chr6:106627696 | T | C | 86 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(83): Show |
92 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+1052A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627696 | |||||||
| chr6:106627702 | C | T | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+1046G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627702 | |||||||
| chr6:106627743 | C | CT | 85 | a0001c0001t0001g0015 a0001c0001t0001g0117 a0001c0001t0001g0118 others(82): Show |
87 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.274+1004dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | |||||||
| chr6:106627743 | C | CTT | 51 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0005g0358 others(48): Show |
56 | HG00438.hp2 HG00738.hp1 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.274+1003_274+1004d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | |||||||
| chr6:106627743 | C | CTTT | 14 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(11): Show |
14 | HG01070.hp2 HG01433.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+1002_274+1004d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | |||||||
| chr6:106627743 | C | CTTTTTTT others(5): Show |
1 | a0001c0002t0001g0008 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.274+993_274+1004du others(13): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | |||||||
| chr6:106627743 | CT | C | 12 | a0001c0001t0001g0274 a0001c0002t0004g0304 a0001c0002t0009g0306 others(9): Show |
12 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.274+1004delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | |||||||
| chr6:106627743 | CTTTTTTT others(3): Show |
C | 3 | a0001c0004t0003g0312 a0001c0005t0008g0310 a0001c0005t0008g0311 |
3 | HG02615.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.274+995_274+1004de others(11): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | |||||||
| chr6:106627743 | CTTTTTTT others(4): Show |
C | 49 | a0001c0004t0003g0002 a0001c0004t0003g0005 a0001c0004t0003g0006 others(46): Show |
57 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.274+994_274+1004de others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | |||||||
| chr6:106627743 | CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0003g0357 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.274+993_274+1004de others(13): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | |||||||
| chr6:106627776 | T | C | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+972A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627776 | |||||||
| chr6:106627805 | T | A | 1 | a0001c0002t0009g0308 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274+943A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627805 | |||||||
| chr6:106627884 | A | G | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.274+864T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627884 | |||||||
| chr6:106628025 | G | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+723C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628025 | |||||||
| chr6:106628050 | G | C | 1 | a0001c0002t0001g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.274+698C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628050 | |||||||
| chr6:106628146 | A | T | 1 | a0001c0008t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+602T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628146 | |||||||
| chr6:106628219 | G | A | 9 | a0001c0003t0006g0023 a0001c0003t0006g0024 a0001c0003t0006g0025 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+529C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628219 | |||||||
| chr6:106628222 | C | G | 1 | a0001c0004t0003g0309 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.274+526G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628222 | |||||||
| chr6:106628237 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.274+511G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628237 | |||||||
| chr6:106628258 | G | A | 1 | a0001c0003t0013g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.274+490C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628258 | |||||||
| chr6:106628467 | CA | C | 10 | a0001c0003t0002g0022 a0001c0003t0006g0023 a0001c0003t0006g0024 others(7): Show |
10 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+280delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628467 | |||||||
| chr6:106628501 | C | G | 1 | a0001c0003t0002g0021 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.274+247G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628501 | |||||||
| chr6:106628562 | C | T | 1 | a0001c0002t0001g0007 | 2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.274+186G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628562 |