Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10313 |
| ensemblid | ENSG00000133318.14 |
| hgncid | 10469 |
| symbol | RTN3 |
| name | reticulon 3 |
| refseq_nuc | NM_001265589.2 |
| refseq_prot | NP_001252518.1 |
| ensembl_nuc | ENST00000377819.10 |
| ensembl_prot | ENSP00000367050.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 63681500 |
| end | 63759882 |
| strand | + |
| ver | v1.2 |
| region | chr11:63681500-63759882 |
| region5000 | chr11:63676500-63764882 |
| regionname0 | RTN3_chr11_63681500_63759882 |
| regionname5000 | RTN3_chr11_63676500_63764882 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1032 | 87 | 17 | 32 | 18 | 7 | 12 | 7 | RTN3_chr11_63676500_63764882 | RTN3 | MAEPS others(1027): Show |
chr11 | 63676500 | 63764882 |
| a0002 | 1/0 | 1032 | 68 | 52 | 8 | 2 | 3 | 2 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | MAEPS others(1027): Show |
chr11 | 63676500 | 63764882 |
| a0003 | 0/0 | 1032 | 11 | 1 | 2 | 0 | 0 | 8 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | MAEPS others(1027): Show |
chr11 | 63676500 | 63764882 |
| a0004 | 0/0 | 1032 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | MAEPS others(1027): Show |
chr11 | 63676500 | 63764882 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3096 | 86 | 17 | 32 | 17 | 7 | 12 | RTN3_chr11_63676500_63764882 | RTN3 | ATGGC others(3091): Show |
chr11 | 63676500 | 63764882 | ||
| a0001c0005 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | ATGGC others(3091): Show |
chr11 | 63676500 | 63764882 | ||
| a0002c0002 | 1/0 | 3096 | 67 | 51 | 8 | 2 | 3 | 2 | RTN3_chr11_63676500_63764882 | RTN3 | ATGGC others(3091): Show |
chr11 | 63676500 | 63764882 | ||
| a0002c0006 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | ATGGC others(3091): Show |
chr11 | 63676500 | 63764882 | ||
| a0003c0003 | 0/0 | 3096 | 11 | 1 | 2 | 0 | 0 | 8 | RTN3_chr11_63676500_63764882 | RTN3 | ATGGC others(3091): Show |
chr11 | 63676500 | 63764882 | ||
| a0004c0004 | 0/0 | 3096 | 4 | 4 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | ATGGC others(3091): Show |
chr11 | 63676500 | 63764882 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4916 | 71 | 17 | 24 | 15 | 4 | 10 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0001c0001t0002 | 0/0 | 4917 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4912): Show |
chr11 | 63676500 | 63764882 |
| a0001c0001t0003 | 0/0 | 4914 | 2 | 0 | 0 | 2 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4909): Show |
chr11 | 63676500 | 63764882 |
| a0001c0001t0007 | 0/0 | 4915 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4910): Show |
chr11 | 63676500 | 63764882 |
| a0001c0001t0008 | 0/0 | 4916 | 6 | 0 | 6 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0001c0001t0010 | 0/0 | 4916 | 2 | 0 | 1 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0001c0001t0012 | 0/0 | 4917 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4912): Show |
chr11 | 63676500 | 63764882 |
| a0001c0001t0013 | 0/0 | 4916 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0001c0001t0014 | 0/0 | 4916 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0001c0005t0001 | 0/0 | 4916 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0001 | 0/0 | 4916 | 22 | 12 | 4 | 2 | 2 | 2 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0002 | 1/0 | 4917 | 10 | 6 | 3 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4912): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0003 | 0/0 | 4914 | 8 | 8 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4909): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0004 | 0/0 | 4919 | 9 | 8 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4914): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0005 | 0/0 | 4916 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0006 | 0/0 | 4915 | 7 | 7 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4910): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0007 | 0/0 | 4915 | 5 | 5 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4910): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0009 | 0/0 | 4917 | 3 | 3 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4912): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0016 | 0/0 | 4915 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4910): Show |
chr11 | 63676500 | 63764882 |
| a0002c0002t0017 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0002c0006t0001 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0003c0003t0001 | 0/0 | 4916 | 2 | 0 | 0 | 0 | 0 | 2 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0003c0003t0005 | 0/0 | 4916 | 6 | 0 | 2 | 0 | 0 | 4 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0003c0003t0011 | 0/0 | 4915 | 2 | 0 | 0 | 0 | 0 | 2 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4910): Show |
chr11 | 63676500 | 63764882 |
| a0003c0003t0015 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| a0004c0004t0001 | 0/0 | 4916 | 4 | 4 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | AGTCT others(4911): Show |
chr11 | 63676500 | 63764882 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0007g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0008g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0008g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0013g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0001t0014g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0001c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0002t0017g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0002c0006t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0005g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0011g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0011g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0003c0003t0015g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0004c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0004c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0004c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| a0004c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0034 | EUR | GBR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00280 | hp1 | a0001 | c0001 | t0012 | g0001 | EUR | FIN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | FIN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00323 | hp1 | a0001 | c0001 | t0010 | g0001 | EUR | FIN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00558 | hp2 | a0001 | c0005 | t0001 | g0109 | EAS | CHS | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00642 | hp2 | a0003 | c0003 | t0005 | g0136 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00738 | hp1 | a0003 | c0003 | t0005 | g0094 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0050 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01109 | hp1 | a0002 | c0002 | t0004 | g0016 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0154 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01255 | hp2 | a0001 | c0001 | t0010 | g0064 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01361 | hp2 | a0001 | c0001 | t0013 | g0129 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0043 | EUR | IBS | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01928 | hp2 | a0001 | c0001 | t0008 | g0047 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0060 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01978 | hp1 | a0001 | c0001 | t0008 | g0049 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01993 | hp2 | a0001 | c0001 | t0008 | g0088 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02145 | hp1 | a0004 | c0004 | t0001 | g0169 | AFR | ACB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02145 | hp2 | a0002 | c0002 | t0006 | g0042 | AFR | ACB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02300 | hp1 | a0001 | c0001 | t0008 | g0131 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02572 | hp1 | a0004 | c0004 | t0001 | g0167 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02572 | hp2 | a0002 | c0002 | t0006 | g0115 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02602 | hp2 | a0001 | c0001 | t0014 | g0127 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02615 | hp1 | a0002 | c0002 | t0016 | g0141 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02622 | hp1 | a0002 | c0002 | t0009 | g0101 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0139 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0105 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02630 | hp2 | a0004 | c0004 | t0001 | g0168 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02647 | hp1 | a0002 | c0002 | t0006 | g0041 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02683 | hp2 | a0003 | c0003 | t0005 | g0096 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02698 | hp1 | a0003 | c0003 | t0011 | g0100 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02717 | hp2 | a0002 | c0002 | t0004 | g0015 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02723 | hp2 | a0002 | c0002 | t0007 | g0002 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0033 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02809 | hp2 | a0004 | c0004 | t0001 | g0166 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0142 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02896 | hp2 | a0002 | c0002 | t0006 | g0158 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02897 | hp1 | a0002 | c0002 | t0007 | g0004 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02897 | hp2 | a0002 | c0002 | t0003 | g0110 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0143 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0151 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03017 | hp1 | a0003 | c0003 | t0011 | g0098 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03041 | hp1 | a0002 | c0002 | t0007 | g0032 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03130 | hp1 | a0002 | c0002 | t0006 | g0144 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03139 | hp1 | a0002 | c0002 | t0009 | g0099 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03195 | hp1 | a0002 | c0002 | t0009 | g0031 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0102 | AFR | ESN | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03209 | hp1 | a0002 | c0002 | t0003 | g0152 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03453 | hp1 | a0002 | c0002 | t0004 | g0011 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0148 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03486 | hp1 | a0002 | c0002 | t0007 | g0005 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0140 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0012 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03540 | hp2 | a0002 | c0002 | t0004 | g0014 | AFR | GWD | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03579 | hp1 | a0002 | c0002 | t0004 | g0017 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0161 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0008 | SAS | STU | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03688 | hp2 | a0003 | c0003 | t0005 | g0097 | SAS | STU | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03710 | hp1 | a0003 | c0003 | t0005 | g0134 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03927 | hp1 | a0003 | c0003 | t0001 | g0009 | SAS | BEB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | BEB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG04184 | hp2 | a0003 | c0003 | t0005 | g0135 | SAS | BEB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18522 | hp1 | a0002 | c0002 | t0007 | g0112 | AFR | YRI | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0010 | AFR | YRI | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA19030 | hp2 | a0002 | c0006 | t0001 | g0145 | AFR | LWK | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA19043 | hp1 | a0002 | c0002 | t0017 | g0003 | AFR | LWK | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0107 | AFR | LWK | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ASW | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA20129 | hp2 | a0002 | c0002 | t0003 | g0147 | AFR | ASW | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA20805 | hp1 | a0002 | c0002 | t0005 | g0095 | EUR | TSI | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0019 | EUR | TSI | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0153 | AFR | ACB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02486 | hp1 | a0002 | c0002 | t0004 | g0018 | AFR | ACB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0106 | AFR | ACB | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG03471 | hp2 | a0002 | c0002 | t0006 | g0111 | AFR | MSL | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | USA | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| HG06807 | hp2 | a0002 | c0002 | t0006 | g0040 | AFR | USA | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA20300 | hp1 | a0003 | c0003 | t0015 | g0093 | AFR | USA | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | USA | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA21309 | hp1 | a0002 | c0002 | t0004 | g0013 | AFR | LWK | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0124 | REF | REF | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0104 | REF | REF | RTN3_chr11_63676500_63764882 | RTN3 | chr11 | 63676500 | 63764882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:63681653 | C | A | 1 | a0003 | 11 | HG00642.hp2 HG00738.hp1 HG02683.hp2 others(8): Show |
missense_variant | MODERATE | c.17C>A | p.Ala6Glu | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/9 | 154/4917 | 17/3099 | 6/1032 | chr11 | 63681653 | |||
| chr11:63719914 | T | C | 2 | a0001 a0004 |
90 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
missense_variant | MODERATE | c.1412T>C | p.Val471Ala | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/9 | 1549/4917 | 1412/3099 | 471/1032 | chr11 | 63719914 | |||
| chr11:63720310 | C | T | 1 | a0004 | 4 | HG02145.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.1808C>T | p.Pro603Leu | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/9 | 1945/4917 | 1808/3099 | 603/1032 | chr11 | 63720310 | |||
| chr11:63759868 | TA | T | 3 | a0001 a0002 a0003 |
23 | HG00642.hp2 HG00738.hp1 HG01516.hp1 others(20): Show |
splice_region_variant | LOW | c.*1681delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 63759868 | ||||||
| chr11:63759868 | TAA | T | 2 | a0001 a0002 |
11 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
splice_region_variant | LOW | c.*1680_*1681delAA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 63759868 | ||||||
| chr11:63759878 | A | AAC | 1 | a0002 | 9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
splice_region_variant | LOW | c.*1678_*1679insCA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 63759878 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:63719828 | A | G | 1 | a0002c0006 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1326A>G | p.Lys442Lys | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/9 | 1463/4917 | 1326/3099 | 442/1032 | chr11 | 63719828 | |||
| chr11:63753669 | G | A | 1 | a0001c0005 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.2955G>A | p.Leu985Leu | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/9 | 3092/4917 | 2955/3099 | 985/1032 | chr11 | 63753669 | |||
| chr11:63753681 | T | C | 1 | a0002c0006 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.2967T>C | p.Ser989Ser | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/9 | 3104/4917 | 2967/3099 | 989/1032 | chr11 | 63753681 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:63758764 | T | C | 2 | a0001c0001t0010 a0001c0001t0012 |
3 | HG00280.hp1 HG00323.hp1 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*563T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | 563 | chr11 | 63758764 | ||||||
| chr11:63758867 | G | A | 1 | a0001c0001t0013 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*666G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | 666 | chr11 | 63758867 | ||||||
| chr11:63758972 | G | A | 1 | a0001c0001t0014 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*771G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | 771 | chr11 | 63758972 | ||||||
| chr11:63759229 | G | A | 5 | a0002c0002t0005 a0002c0002t0009 a0003c0003t0005 others(2): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1028G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | 1028 | chr11 | 63759229 | ||||||
| chr11:63759519 | C | T | 1 | a0001c0001t0008 | 6 | HG01074.hp2 HG01928.hp2 HG01975.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1318C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | 1318 | chr11 | 63759519 | ||||||
| chr11:63759688 | G | A | 1 | a0002c0002t0006 | 7 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1487G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | 1487 | chr11 | 63759688 | ||||||
| chr11:63759719 | AT | A | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(14): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1533delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 9/9 | 1533 | INFO_REALIGN_3_PRIME | chr11 | 63759719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:63682170 | T | C | 4 | a0002c0002t0007g0002 a0002c0002t0007g0004 a0002c0002t0007g0005 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+392T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63682170 | |||||||
| chr11:63682331 | G | T | 4 | a0004c0004t0001g0166 a0004c0004t0001g0167 a0004c0004t0001g0168 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+553G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63682331 | |||||||
| chr11:63682744 | T | C | 1 | a0002c0002t0007g0002 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142+966T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63682744 | |||||||
| chr11:63682843 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142+1065A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63682843 | |||||||
| chr11:63682858 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.142+1080T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63682858 | |||||||
| chr11:63682907 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.142+1129A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63682907 | |||||||
| chr11:63683065 | C | T | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.142+1287C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63683065 | |||||||
| chr11:63683284 | A | C | 3 | a0002c0002t0001g0160 a0002c0002t0001g0161 a0002c0002t0001g0162 |
3 | HG01934.hp2 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.142+1506A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63683284 | |||||||
| chr11:63683313 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.142+1535A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63683313 | |||||||
| chr11:63683386 | T | G | 1 | a0001c0001t0001g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.142+1608T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63683386 | |||||||
| chr11:63683790 | A | G | 1 | a0002c0002t0006g0158 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.142+2012A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63683790 | |||||||
| chr11:63683943 | C | CT | 37 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(34): Show |
37 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.142+2194dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63683943 | ||||||
| chr11:63683943 | C | CTT | 7 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0002c0002t0002g0151 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.142+2193_142+2194d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63683943 | ||||||
| chr11:63683943 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.142+2185_142+2194d others(12): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63683943 | ||||||
| chr11:63683943 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.142+2184_142+2194d others(13): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63683943 | ||||||
| chr11:63683943 | CT | C | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0025 others(11): Show |
14 | HG00099.hp1 HG00323.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+2194delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63683943 | ||||||
| chr11:63683943 | CTTTTTTT others(4): Show |
C | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+2184_142+2194d others(13): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63683943 | ||||||
| chr11:63683947 | T | C | 2 | a0003c0003t0001g0008 a0003c0003t0001g0009 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.142+2169T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63683947 | |||||||
| chr11:63683972 | T | A | 1 | a0002c0002t0001g0019 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.142+2194T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63683972 | |||||||
| chr11:63683972 | T | TA | 7 | a0002c0002t0001g0033 a0002c0002t0001g0034 a0002c0002t0001g0037 others(4): Show |
7 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+2195dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63683972 | ||||||
| chr11:63683982 | C | A | 4 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+2204C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63683982 | |||||||
| chr11:63684129 | G | GT | 20 | a0002c0002t0001g0019 a0002c0002t0001g0039 a0002c0002t0001g0113 others(17): Show |
20 | HG01243.hp1 HG02071.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.142+2376dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63684129 | ||||||
| chr11:63684129 | G | GTT | 7 | a0002c0002t0003g0147 a0002c0002t0003g0148 a0002c0002t0006g0041 others(4): Show |
7 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+2375_142+2376d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63684129 | ||||||
| chr11:63684129 | GT | G | 5 | a0002c0002t0009g0101 a0003c0003t0001g0008 a0003c0003t0005g0135 others(2): Show |
5 | HG00642.hp2 HG02622.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+2376delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63684129 | ||||||
| chr11:63684129 | GTT | G | 9 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(6): Show |
9 | HG00738.hp1 HG02683.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+2375_142+2376d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63684129 | ||||||
| chr11:63684129 | GTTTTT | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(12): Show |
15 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.142+2372_142+2376d others(7): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63684129 | ||||||
| chr11:63684129 | GTTTTTT | G | 84 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0025 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.142+2371_142+2376d others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63684129 | ||||||
| chr11:63684129 | GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0159 |
3 | HG01516.hp2 HG02015.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.142+2367_142+2376d others(12): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63684129 | ||||||
| chr11:63684135 | T | G | 1 | a0001c0001t0007g0043 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.142+2357T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684135 | |||||||
| chr11:63684142 | T | G | 1 | a0002c0002t0001g0020 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.142+2364T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684142 | |||||||
| chr11:63684152 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
5 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+2374T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684152 | |||||||
| chr11:63684154 | T | G | 15 | a0001c0001t0001g0130 a0001c0001t0008g0088 a0002c0002t0005g0095 others(12): Show |
15 | HG00642.hp2 HG00738.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.142+2376T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684154 | |||||||
| chr11:63684156 | G | T | 15 | a0001c0001t0001g0130 a0001c0001t0008g0088 a0002c0002t0005g0095 others(12): Show |
15 | HG00642.hp2 HG00738.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.142+2378G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684156 | |||||||
| chr11:63684165 | T | G | 1 | a0002c0002t0016g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.142+2387T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684165 | |||||||
| chr11:63684180 | G | A | 1 | a0003c0003t0015g0093 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.142+2402G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684180 | |||||||
| chr11:63684307 | C | T | 2 | a0003c0003t0001g0008 a0003c0003t0001g0009 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.142+2529C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684307 | |||||||
| chr11:63684628 | A | T | 90 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(87): Show |
90 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.142+2850A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684628 | |||||||
| chr11:63684658 | G | A | 1 | a0002c0002t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.142+2880G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684658 | |||||||
| chr11:63684839 | A | C | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+3061A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684839 | |||||||
| chr11:63684878 | G | C | 8 | a0002c0002t0003g0110 a0002c0002t0003g0142 a0002c0002t0003g0143 others(5): Show |
8 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+3100G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684878 | |||||||
| chr11:63684910 | C | T | 1 | a0002c0002t0016g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.142+3132C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63684910 | |||||||
| chr11:63685012 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0008g0047 a0001c0001t0008g0049 others(3): Show |
6 | HG01074.hp2 HG01928.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+3234G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685012 | |||||||
| chr11:63685029 | G | A | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+3251G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685029 | |||||||
| chr11:63685034 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.142+3256A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685034 | |||||||
| chr11:63685104 | C | G | 1 | a0002c0002t0004g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+3326C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685104 | |||||||
| chr11:63685331 | C | G | 2 | a0001c0001t0001g0087 a0001c0001t0013g0129 |
2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.142+3553C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685331 | |||||||
| chr11:63685419 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.142+3641C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685419 | |||||||
| chr11:63685437 | A | AGT | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+3661_142+3662d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685437 | ||||||
| chr11:63685491 | A | G | 13 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(10): Show |
13 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+3713A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685491 | |||||||
| chr11:63685495 | C | CAAA | 91 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(88): Show |
91 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.142+3729_142+3731d others(5): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(1): Show |
6 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(3): Show |
6 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+3724_142+3731d others(10): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(6): Show |
15 | a0002c0002t0001g0038 a0002c0002t0001g0113 a0002c0002t0005g0095 others(12): Show |
15 | HG00642.hp2 HG00738.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.142+3719_142+3731d others(15): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(7): Show |
4 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 others(1): Show |
4 | HG02717.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+3718_142+3731d others(16): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(8): Show |
6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+3731_142+3732i others(17): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(9): Show |
3 | a0002c0002t0003g0143 a0002c0002t0003g0153 a0002c0002t0016g0141 |
3 | HG02109.hp2 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.142+3731_142+3732i others(18): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(14): Show |
1 | a0002c0002t0001g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142+3731_142+3732i others(23): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(15): Show |
2 | a0003c0003t0001g0008 a0003c0003t0001g0009 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.142+3731_142+3732i others(24): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(16): Show |
5 | a0002c0002t0001g0102 a0002c0002t0001g0137 a0002c0002t0001g0138 others(2): Show |
5 | HG02886.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+3731_142+3732i others(25): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(17): Show |
4 | a0002c0002t0001g0149 a0002c0002t0007g0032 a0002c0002t0007g0112 others(1): Show |
4 | HG01109.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+3731_142+3732i others(26): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(18): Show |
4 | a0002c0002t0003g0148 a0002c0002t0007g0002 a0002c0002t0007g0004 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+3731_142+3732i others(27): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(19): Show |
6 | a0002c0002t0001g0019 a0002c0002t0003g0142 a0002c0002t0003g0147 others(3): Show |
6 | HG02896.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+3731_142+3732i others(28): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(20): Show |
2 | a0002c0002t0003g0110 a0002c0002t0006g0041 |
2 | HG02647.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.142+3731_142+3732i others(29): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(23): Show |
1 | a0002c0002t0006g0111 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142+3731_142+3732i others(32): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(24): Show |
2 | a0002c0002t0001g0037 a0002c0002t0006g0144 |
2 | HG01433.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+3731_142+3732i others(33): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(25): Show |
1 | a0002c0002t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.142+3731_142+3732i others(34): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(26): Show |
1 | a0002c0002t0002g0036 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.142+3731_142+3732i others(35): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(27): Show |
1 | a0002c0002t0002g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.142+3731_142+3732i others(36): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(29): Show |
1 | a0002c0002t0006g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+3731_142+3732i others(38): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(30): Show |
1 | a0002c0002t0001g0034 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.142+3731_142+3732i others(39): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685495 | C | CAAAAAAA others(34): Show |
1 | a0002c0002t0001g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.142+3731_142+3732i others(43): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63685495 | ||||||
| chr11:63685565 | A | G | 1 | a0002c0002t0001g0162 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.142+3787A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685565 | |||||||
| chr11:63685648 | C | T | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+3870C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685648 | |||||||
| chr11:63685704 | T | C | 153 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(150): Show |
153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.142+3926T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63685704 | |||||||
| chr11:63686271 | T | C | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.142+4493T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63686271 | |||||||
| chr11:63686344 | G | C | 2 | a0001c0001t0010g0001 a0001c0001t0012g0001 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.142+4566G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63686344 | |||||||
| chr11:63686361 | C | G | 1 | a0002c0002t0003g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142+4583C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63686361 | |||||||
| chr11:63686453 | AGAGCGAG others(3): Show |
A | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+4676_142+4685d others(12): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63686453 | |||||||
| chr11:63686470 | CA | C | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.142+4712delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63686470 | ||||||
| chr11:63686470 | CAAAAA | C | 25 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(22): Show |
25 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.142+4708_142+4712d others(7): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63686470 | ||||||
| chr11:63686504 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.142+4726A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63686504 | |||||||
| chr11:63686572 | C | G | 1 | a0004c0004t0001g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.142+4794C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63686572 | |||||||
| chr11:63686705 | C | T | 3 | a0002c0002t0003g0110 a0002c0002t0003g0142 a0002c0002t0003g0147 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142+4927C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63686705 | |||||||
| chr11:63686771 | C | G | 1 | a0002c0002t0007g0004 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.142+4993C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63686771 | |||||||
| chr11:63687260 | G | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+5482G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63687260 | |||||||
| chr11:63687462 | C | CA | 4 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0149 others(1): Show |
4 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+5690dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63687462 | ||||||
| chr11:63687608 | TA | T | 10 | a0001c0001t0001g0022 a0002c0002t0004g0010 a0002c0002t0004g0011 others(7): Show |
10 | HG00323.hp2 HG01109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.142+5845delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63687608 | ||||||
| chr11:63687667 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0083 others(2): Show |
5 | HG00642.hp1 HG01123.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+5889A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63687667 | |||||||
| chr11:63687890 | T | C | 1 | a0002c0002t0007g0112 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.142+6112T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63687890 | |||||||
| chr11:63688004 | G | C | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+6226G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63688004 | |||||||
| chr11:63688064 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.142+6286A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63688064 | |||||||
| chr11:63688121 | G | A | 1 | a0002c0002t0007g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+6343G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63688121 | |||||||
| chr11:63688162 | G | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142+6384G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63688162 | |||||||
| chr11:63688223 | C | CT | 45 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0029 others(42): Show |
45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.142+6463dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63688223 | ||||||
| chr11:63688223 | C | CTT | 9 | a0001c0001t0001g0130 a0002c0002t0001g0163 a0002c0002t0006g0040 others(6): Show |
9 | HG01361.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+6462_142+6463d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63688223 | ||||||
| chr11:63688405 | G | A | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+6627G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63688405 | |||||||
| chr11:63688464 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.142+6686C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63688464 | |||||||
| chr11:63688630 | T | G | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+6852T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63688630 | |||||||
| chr11:63689006 | T | G | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+7228T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63689006 | |||||||
| chr11:63689373 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+7595A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63689373 | |||||||
| chr11:63689599 | A | AT | 14 | a0002c0002t0003g0148 a0002c0002t0006g0040 a0002c0002t0006g0041 others(11): Show |
14 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.142+7833dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63689599 | ||||||
| chr11:63689785 | T | C | 10 | a0002c0002t0005g0095 a0003c0003t0005g0094 a0003c0003t0005g0096 others(7): Show |
10 | HG00642.hp2 HG00738.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+8007T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63689785 | |||||||
| chr11:63689851 | G | A | 3 | a0002c0002t0009g0031 a0002c0002t0009g0099 a0002c0002t0009g0101 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.142+8073G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63689851 | |||||||
| chr11:63689866 | T | C | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142+8088T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63689866 | |||||||
| chr11:63689977 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0003g0117 |
2 | NA18964.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.142+8199C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63689977 | |||||||
| chr11:63690067 | A | G | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+8289A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63690067 | |||||||
| chr11:63690090 | A | G | 1 | a0001c0001t0014g0127 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.142+8312A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63690090 | |||||||
| chr11:63690539 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.142+8761G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63690539 | |||||||
| chr11:63690681 | G | A | 13 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(10): Show |
13 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+8903G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63690681 | |||||||
| chr11:63690845 | C | T | 2 | a0002c0002t0003g0148 a0002c0002t0003g0152 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.142+9067C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63690845 | |||||||
| chr11:63691114 | C | CT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0074 others(20): Show |
23 | HG00642.hp2 HG01106.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.142+9360dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63691114 | ||||||
| chr11:63691114 | C | CTT | 5 | a0001c0001t0001g0077 a0002c0002t0001g0149 a0002c0002t0004g0011 others(2): Show |
5 | HG01109.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+9359_142+9360d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63691114 | ||||||
| chr11:63691174 | G | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142+9396G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63691174 | |||||||
| chr11:63691223 | C | T | 1 | a0003c0003t0015g0093 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.142+9445C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63691223 | |||||||
| chr11:63691726 | A | G | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+9948A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63691726 | |||||||
| chr11:63691759 | A | T | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142+9981A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63691759 | |||||||
| chr11:63692286 | G | T | 1 | a0002c0002t0007g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+10508G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63692286 | |||||||
| chr11:63692407 | G | A | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+10629G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63692407 | |||||||
| chr11:63692653 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.142+10875C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63692653 | |||||||
| chr11:63692814 | TTTTC | T | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+11040_142+1104 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63692814 | ||||||
| chr11:63692939 | GAGAA | G | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+11167_142+1117 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63692939 | ||||||
| chr11:63693157 | G | A | 1 | a0002c0002t0002g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.142+11379G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63693157 | |||||||
| chr11:63693255 | G | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+11477G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63693255 | |||||||
| chr11:63693282 | G | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0085 others(3): Show |
6 | HG01243.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+11504G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63693282 | |||||||
| chr11:63693339 | T | C | 59 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(56): Show |
59 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.143-11512T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63693339 | |||||||
| chr11:63693438 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.143-11413C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63693438 | |||||||
| chr11:63693439 | G | A | 1 | a0002c0002t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.143-11412G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63693439 | |||||||
| chr11:63693699 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.143-11152T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63693699 | |||||||
| chr11:63693981 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.143-10870G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63693981 | |||||||
| chr11:63694149 | T | C | 1 | a0002c0002t0003g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.143-10702T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63694149 | |||||||
| chr11:63694164 | TATTA | T | 2 | a0002c0002t0002g0151 a0002c0002t0002g0154 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.143-10678_143-1067 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63694164 | ||||||
| chr11:63694179 | G | A | 11 | a0002c0002t0001g0163 a0002c0002t0002g0151 a0002c0002t0002g0154 others(8): Show |
11 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-10672G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63694179 | |||||||
| chr11:63694233 | A | G | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.143-10618A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63694233 | |||||||
| chr11:63694324 | G | A | 3 | a0002c0002t0009g0031 a0002c0002t0009g0099 a0002c0002t0009g0101 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.143-10527G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63694324 | |||||||
| chr11:63694355 | T | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0092 a0001c0001t0001g0108 |
3 | HG00558.hp1 HG00621.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.143-10496T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63694355 | |||||||
| chr11:63694631 | G | C | 3 | a0002c0002t0001g0163 a0002c0002t0002g0151 a0002c0002t0002g0154 |
3 | HG01243.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.143-10220G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63694631 | |||||||
| chr11:63694748 | G | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0132 a0002c0002t0004g0014 others(2): Show |
5 | HG02717.hp2 HG03209.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-10103G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63694748 | |||||||
| chr11:63695326 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-9525A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63695326 | |||||||
| chr11:63695335 | G | T | 1 | a0002c0002t0003g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.143-9516G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63695335 | |||||||
| chr11:63695565 | C | T | 2 | a0002c0002t0003g0143 a0002c0002t0016g0141 |
2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.143-9286C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63695565 | |||||||
| chr11:63695804 | C | A | 1 | a0002c0002t0003g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143-9047C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63695804 | |||||||
| chr11:63696092 | T | TA | 22 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(19): Show |
22 | HG00642.hp2 HG00738.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.143-8743dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63696092 | ||||||
| chr11:63696092 | TA | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0084 a0002c0002t0001g0160 others(6): Show |
9 | HG00642.hp1 HG01934.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-8743delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63696092 | ||||||
| chr11:63696197 | T | C | 4 | a0002c0002t0001g0102 a0002c0002t0001g0103 a0003c0003t0001g0008 others(1): Show |
4 | HG03098.hp1 HG03195.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-8654T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696197 | |||||||
| chr11:63696225 | C | T | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-8626C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696225 | |||||||
| chr11:63696233 | C | G | 1 | a0002c0002t0007g0002 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-8618C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696233 | |||||||
| chr11:63696465 | C | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0085 others(3): Show |
6 | HG01243.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-8386C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696465 | |||||||
| chr11:63696465 | C | T | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.143-8386C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696465 | |||||||
| chr11:63696541 | C | T | 1 | a0003c0003t0001g0008 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.143-8310C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696541 | |||||||
| chr11:63696543 | A | AT | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.143-8289dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63696543 | ||||||
| chr11:63696543 | A | ATT | 12 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0125 others(9): Show |
12 | HG00558.hp2 HG00597.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-8290_143-8289d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63696543 | ||||||
| chr11:63696543 | AT | A | 31 | a0002c0002t0001g0163 a0002c0002t0002g0139 a0002c0002t0002g0151 others(28): Show |
31 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.143-8289delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63696543 | ||||||
| chr11:63696569 | G | A | 1 | a0002c0002t0006g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.143-8282G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696569 | |||||||
| chr11:63696626 | A | G | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-8225A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696626 | |||||||
| chr11:63696857 | TTTTC | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.143-7970_143-7967d others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63696857 | ||||||
| chr11:63696857 | TTTTCTTT others(9): Show |
T | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-7982_143-7967d others(18): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63696857 | ||||||
| chr11:63696878 | TTTC | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0002c0002t0004g0010 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-7970_143-7968d others(5): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63696878 | ||||||
| chr11:63696879 | TTC | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.143-7970_143-7969d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63696879 | ||||||
| chr11:63696880 | TC | T | 18 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(15): Show |
18 | HG01106.hp2 HG01109.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.143-7970delC | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696880 | |||||||
| chr11:63696881 | C | T | 2 | a0002c0002t0001g0146 a0002c0002t0016g0141 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.143-7970C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696881 | |||||||
| chr11:63696946 | G | A | 5 | a0002c0002t0003g0110 a0002c0002t0003g0142 a0002c0002t0003g0147 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-7905G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696946 | |||||||
| chr11:63696953 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.143-7898T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696953 | |||||||
| chr11:63696961 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.143-7890G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63696961 | |||||||
| chr11:63697028 | A | G | 35 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(32): Show |
35 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.143-7823A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63697028 | |||||||
| chr11:63697253 | C | CACGAATG | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-7596_143-7595i others(9): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63697253 | ||||||
| chr11:63697314 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.143-7537A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63697314 | |||||||
| chr11:63697324 | G | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-7527G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63697324 | |||||||
| chr11:63697336 | C | T | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-7515C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63697336 | |||||||
| chr11:63697469 | C | CATTATT | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(91): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.143-7366_143-7361d others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63697469 | ||||||
| chr11:63697473 | A | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-7378A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63697473 | |||||||
| chr11:63698212 | T | C | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.143-6639T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63698212 | |||||||
| chr11:63698573 | A | G | 1 | a0003c0003t0001g0009 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.143-6278A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63698573 | |||||||
| chr11:63698645 | C | T | 2 | a0002c0002t0002g0151 a0002c0002t0002g0154 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.143-6206C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63698645 | |||||||
| chr11:63698667 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.143-6184A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63698667 | |||||||
| chr11:63698723 | G | A | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-6128G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63698723 | |||||||
| chr11:63699025 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.143-5826C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63699025 | |||||||
| chr11:63699037 | G | A | 10 | a0002c0002t0005g0095 a0003c0003t0005g0094 a0003c0003t0005g0096 others(7): Show |
10 | HG00642.hp2 HG00738.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-5814G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63699037 | |||||||
| chr11:63699045 | T | C | 10 | a0002c0002t0005g0095 a0003c0003t0005g0094 a0003c0003t0005g0096 others(7): Show |
10 | HG00642.hp2 HG00738.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-5806T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63699045 | |||||||
| chr11:63699060 | G | A | 1 | a0003c0003t0005g0136 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.143-5791G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63699060 | |||||||
| chr11:63699216 | A | T | 33 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(30): Show |
33 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.143-5635A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63699216 | |||||||
| chr11:63699233 | G | A | 2 | a0002c0002t0005g0095 a0003c0003t0005g0094 |
2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.143-5618G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63699233 | |||||||
| chr11:63699433 | C | T | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-5418C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63699433 | |||||||
| chr11:63699454 | C | A | 1 | a0002c0002t0001g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.143-5397C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63699454 | |||||||
| chr11:63700183 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.143-4668A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63700183 | |||||||
| chr11:63700192 | C | A | 13 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(10): Show |
13 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-4659C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63700192 | |||||||
| chr11:63700282 | C | CTTTTTTT others(4): Show |
26 | a0002c0002t0001g0102 a0002c0002t0001g0137 a0002c0002t0001g0138 others(23): Show |
26 | HG01109.hp1 HG01109.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.143-4568_143-4558d others(13): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63700282 | ||||||
| chr11:63700282 | C | CTTTTTTT others(5): Show |
3 | a0002c0002t0004g0013 a0002c0002t0006g0041 a0002c0002t0006g0042 |
3 | HG02145.hp2 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.143-4558_143-4557i others(14): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63700282 | ||||||
| chr11:63700564 | G | A | 2 | a0002c0002t0001g0160 a0002c0002t0001g0161 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143-4287G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63700564 | |||||||
| chr11:63700612 | T | A | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-4239T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63700612 | |||||||
| chr11:63700694 | C | G | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-4157C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63700694 | |||||||
| chr11:63700882 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.143-3969G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63700882 | |||||||
| chr11:63700962 | C | T | 1 | a0004c0004t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.143-3889C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63700962 | |||||||
| chr11:63700996 | A | G | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
6 | HG01106.hp2 HG01192.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-3855A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63700996 | |||||||
| chr11:63701088 | C | CA | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(85): Show |
88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.143-3748dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63701088 | ||||||
| chr11:63701088 | CAA | C | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-3749_143-3748d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63701088 | ||||||
| chr11:63701201 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.143-3650A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63701201 | |||||||
| chr11:63701290 | G | T | 1 | a0002c0002t0004g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.143-3561G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63701290 | |||||||
| chr11:63701563 | C | T | 2 | a0002c0002t0003g0148 a0002c0002t0003g0152 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.143-3288C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63701563 | |||||||
| chr11:63702173 | GTATT | G | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-2675_143-2672d others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63702173 | ||||||
| chr11:63702297 | G | T | 1 | a0003c0003t0001g0009 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.143-2554G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63702297 | |||||||
| chr11:63702322 | G | GT | 11 | a0001c0001t0001g0130 a0002c0002t0006g0040 a0002c0002t0006g0041 others(8): Show |
11 | HG00642.hp2 HG01361.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-2519dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63702322 | ||||||
| chr11:63702472 | G | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-2379G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63702472 | |||||||
| chr11:63702497 | G | A | 1 | a0002c0002t0007g0112 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.143-2354G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63702497 | |||||||
| chr11:63702521 | G | A | 1 | a0002c0002t0001g0034 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.143-2330G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63702521 | |||||||
| chr11:63702609 | C | T | 1 | a0003c0003t0005g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.143-2242C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63702609 | |||||||
| chr11:63702692 | GT | G | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.143-2148delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63702692 | ||||||
| chr11:63702709 | G | A | 2 | a0002c0002t0002g0151 a0002c0002t0002g0154 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.143-2142G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63702709 | |||||||
| chr11:63702778 | T | C | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-2073T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63702778 | |||||||
| chr11:63702954 | G | A | 1 | a0002c0002t0004g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.143-1897G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63702954 | |||||||
| chr11:63702970 | C | G | 1 | a0002c0002t0002g0105 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.143-1881C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63702970 | |||||||
| chr11:63703288 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143-1563G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63703288 | |||||||
| chr11:63703370 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.143-1481G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63703370 | |||||||
| chr11:63703692 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.143-1159G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63703692 | |||||||
| chr11:63703743 | C | T | 1 | a0002c0002t0004g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.143-1108C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63703743 | |||||||
| chr11:63703744 | G | A | 1 | a0002c0006t0001g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.143-1107G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63703744 | |||||||
| chr11:63703996 | T | C | 1 | a0002c0002t0007g0112 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.143-855T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63703996 | |||||||
| chr11:63704375 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.143-476A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | chr11 | 63704375 | |||||||
| chr11:63704620 | TA | T | 10 | a0001c0001t0001g0063 a0001c0001t0001g0121 a0002c0002t0001g0137 others(7): Show |
10 | HG01074.hp1 HG01109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.143-218delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 63704620 | ||||||
| chr11:63705227 | C | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.199+320C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63705227 | |||||||
| chr11:63705300 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.199+393C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63705300 | |||||||
| chr11:63705977 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0008g0047 a0001c0001t0008g0049 others(3): Show |
6 | HG01074.hp2 HG01928.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+1070A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63705977 | |||||||
| chr11:63706230 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.199+1323G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63706230 | |||||||
| chr11:63706348 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0123 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.199+1441C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63706348 | |||||||
| chr11:63706348 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.199+1441C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63706348 | |||||||
| chr11:63706888 | T | C | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199+1981T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63706888 | |||||||
| chr11:63706901 | C | CT | 9 | a0002c0002t0001g0163 a0002c0002t0002g0151 a0002c0002t0002g0154 others(6): Show |
9 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.199+2007dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63706901 | ||||||
| chr11:63706901 | CT | C | 29 | a0001c0001t0001g0057 a0002c0002t0001g0020 a0002c0002t0001g0023 others(26): Show |
29 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.199+2007delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63706901 | ||||||
| chr11:63707087 | C | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+2180C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63707087 | |||||||
| chr11:63707188 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.199+2281G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63707188 | |||||||
| chr11:63707190 | C | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+2283C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63707190 | |||||||
| chr11:63707251 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.199+2344C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63707251 | |||||||
| chr11:63707282 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.199+2375A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63707282 | |||||||
| chr11:63707331 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.199+2424T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63707331 | |||||||
| chr11:63707487 | A | T | 3 | a0002c0002t0003g0110 a0002c0002t0003g0142 a0002c0002t0003g0147 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.199+2580A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63707487 | |||||||
| chr11:63707760 | G | C | 1 | a0003c0003t0011g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.199+2853G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63707760 | |||||||
| chr11:63707974 | G | A | 1 | a0002c0002t0007g0112 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.199+3067G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63707974 | |||||||
| chr11:63708002 | G | C | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.199+3095G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63708002 | |||||||
| chr11:63708317 | G | A | 1 | a0002c0002t0006g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.199+3410G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63708317 | |||||||
| chr11:63708548 | G | T | 1 | a0001c0001t0008g0050 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.199+3641G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63708548 | |||||||
| chr11:63708835 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.199+3928A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63708835 | |||||||
| chr11:63709471 | T | C | 1 | a0002c0002t0004g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.199+4564T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63709471 | |||||||
| chr11:63709514 | G | A | 1 | a0001c0001t0008g0088 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.199+4607G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63709514 | |||||||
| chr11:63709584 | TA | T | 41 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0062 others(38): Show |
41 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.199+4690delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63709584 | ||||||
| chr11:63709585 | A | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.199+4678A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63709585 | |||||||
| chr11:63709586 | A | G | 1 | a0003c0003t0011g0098 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.199+4679A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63709586 | |||||||
| chr11:63709586 | A | T | 26 | a0001c0001t0001g0025 a0001c0001t0001g0052 a0001c0001t0001g0057 others(23): Show |
26 | HG01169.hp2 HG01433.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.199+4679A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63709586 | |||||||
| chr11:63709807 | G | A | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.199+4900G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63709807 | |||||||
| chr11:63709899 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.199+4992T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63709899 | |||||||
| chr11:63710357 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.199+5450T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63710357 | |||||||
| chr11:63710471 | GT | G | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+5571delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63710471 | ||||||
| chr11:63710619 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.199+5712G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63710619 | |||||||
| chr11:63710639 | G | A | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.199+5732G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63710639 | |||||||
| chr11:63710703 | A | AC | 5 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0090 others(2): Show |
5 | HG01106.hp1 HG01192.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+5796_199+5797i others(3): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63710703 | |||||||
| chr11:63710705 | A | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0090 others(2): Show |
5 | HG01106.hp1 HG01192.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+5798A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63710705 | |||||||
| chr11:63710888 | G | T | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.199+5981G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63710888 | |||||||
| chr11:63711107 | C | T | 1 | a0002c0002t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.199+6200C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63711107 | |||||||
| chr11:63711384 | A | AT | 14 | a0001c0001t0001g0086 a0002c0002t0005g0095 a0002c0002t0009g0031 others(11): Show |
14 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+6487dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63711384 | ||||||
| chr11:63711392 | T | G | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+6485T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63711392 | |||||||
| chr11:63711585 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.199+6678C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63711585 | |||||||
| chr11:63711936 | A | G | 32 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0029 others(29): Show |
32 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.200-6766A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63711936 | |||||||
| chr11:63711985 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.200-6717C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63711985 | |||||||
| chr11:63712483 | AT | A | 150 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.200-6199delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63712483 | ||||||
| chr11:63712483 | ATT | A | 8 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0071 others(5): Show |
8 | HG00558.hp1 HG00558.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-6200_200-6199d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63712483 | ||||||
| chr11:63712588 | C | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-6114C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63712588 | |||||||
| chr11:63712703 | T | C | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.200-5999T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63712703 | |||||||
| chr11:63712775 | G | A | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.200-5927G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63712775 | |||||||
| chr11:63712921 | C | T | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.200-5781C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63712921 | |||||||
| chr11:63713445 | G | A | 1 | a0001c0005t0001g0109 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.200-5257G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63713445 | |||||||
| chr11:63713482 | T | A | 1 | a0001c0001t0013g0129 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.200-5220T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63713482 | |||||||
| chr11:63713775 | G | A | 4 | a0002c0002t0007g0002 a0002c0002t0007g0004 a0002c0002t0007g0005 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-4927G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63713775 | |||||||
| chr11:63713846 | A | G | 4 | a0002c0002t0007g0002 a0002c0002t0007g0004 a0002c0002t0007g0005 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-4856A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63713846 | |||||||
| chr11:63714566 | G | A | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-4136G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63714566 | |||||||
| chr11:63714932 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.200-3770T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63714932 | |||||||
| chr11:63714938 | CT | C | 3 | a0002c0002t0009g0031 a0002c0002t0009g0099 a0002c0002t0009g0101 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.200-3760delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63714938 | ||||||
| chr11:63715059 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.200-3643C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63715059 | |||||||
| chr11:63715295 | A | G | 2 | a0002c0002t0002g0151 a0002c0002t0002g0154 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.200-3407A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63715295 | |||||||
| chr11:63715658 | AAAAAAAC others(4): Show |
A | 9 | a0002c0002t0005g0095 a0003c0003t0005g0094 a0003c0003t0005g0096 others(6): Show |
9 | HG00642.hp2 HG00738.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.200-3026_200-3016d others(13): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63715658 | ||||||
| chr11:63715682 | A | C | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.200-3020A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63715682 | |||||||
| chr11:63715719 | G | A | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-2983G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63715719 | |||||||
| chr11:63715912 | T | G | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-2790T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63715912 | |||||||
| chr11:63716104 | A | G | 97 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(94): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.200-2598A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716104 | |||||||
| chr11:63716216 | A | G | 1 | a0002c0002t0001g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.200-2486A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716216 | |||||||
| chr11:63716544 | G | A | 13 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(10): Show |
13 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.200-2158G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716544 | |||||||
| chr11:63716603 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.200-2099G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716603 | |||||||
| chr11:63716888 | G | A | 11 | a0002c0002t0001g0163 a0002c0002t0002g0151 a0002c0002t0002g0154 others(8): Show |
11 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.200-1814G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716888 | |||||||
| chr11:63716894 | G | A | 13 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(10): Show |
13 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-1808G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716894 | |||||||
| chr11:63716926 | G | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-1776G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716926 | |||||||
| chr11:63716963 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.200-1739C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716963 | |||||||
| chr11:63716968 | C | CA | 7 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(4): Show |
7 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.200-1724dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63716968 | ||||||
| chr11:63716978 | A | AAC | 10 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(7): Show |
10 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.200-1724_200-1723i others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716978 | |||||||
| chr11:63716979 | C | A | 10 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(7): Show |
10 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.200-1723C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63716979 | |||||||
| chr11:63716979 | C | CA | 22 | a0002c0002t0002g0151 a0002c0002t0002g0154 a0002c0002t0003g0110 others(19): Show |
22 | HG00642.hp2 HG00738.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.200-1707dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63716979 | ||||||
| chr11:63716979 | C | CAA | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(89): Show |
92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.200-1708_200-1707d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63716979 | ||||||
| chr11:63717216 | T | G | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-1486T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63717216 | |||||||
| chr11:63717375 | C | CT | 29 | a0001c0001t0001g0007 a0001c0001t0001g0056 a0001c0001t0001g0059 others(26): Show |
29 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.200-1300dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63717375 | ||||||
| chr11:63717375 | CT | C | 8 | a0001c0001t0001g0051 a0001c0001t0001g0083 a0001c0001t0001g0156 others(5): Show |
8 | HG01243.hp1 HG01952.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.200-1300delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63717375 | ||||||
| chr11:63717375 | CTT | C | 7 | a0002c0002t0003g0110 a0002c0002t0003g0142 a0002c0002t0003g0147 others(4): Show |
7 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.200-1301_200-1300d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63717375 | ||||||
| chr11:63717375 | CTTT | C | 11 | a0002c0002t0003g0143 a0002c0002t0003g0153 a0002c0002t0005g0095 others(8): Show |
11 | HG00642.hp2 HG00738.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.200-1302_200-1300d others(5): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63717375 | ||||||
| chr11:63717375 | CTTTT | C | 18 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0002c0002t0001g0020 others(15): Show |
18 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-1303_200-1300d others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63717375 | ||||||
| chr11:63717404 | A | G | 1 | a0001c0001t0003g0117 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.200-1298A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63717404 | |||||||
| chr11:63717435 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.200-1267G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63717435 | |||||||
| chr11:63717446 | T | C | 13 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(10): Show |
13 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.200-1256T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63717446 | |||||||
| chr11:63717715 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.200-987A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63717715 | |||||||
| chr11:63717973 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.200-729C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63717973 | |||||||
| chr11:63718015 | C | CA | 8 | a0001c0001t0001g0120 a0002c0002t0004g0010 a0002c0002t0004g0011 others(5): Show |
8 | HG01109.hp1 HG02300.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-671dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63718015 | ||||||
| chr11:63718015 | CA | C | 14 | a0001c0001t0001g0054 a0002c0002t0005g0095 a0002c0002t0009g0031 others(11): Show |
14 | HG00642.hp2 HG00738.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.200-671delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 63718015 | ||||||
| chr11:63718099 | A | G | 13 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(10): Show |
13 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-603A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63718099 | |||||||
| chr11:63718265 | A | G | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-437A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63718265 | |||||||
| chr11:63718344 | G | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-358G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63718344 | |||||||
| chr11:63718478 | T | C | 162 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.200-224T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63718478 | |||||||
| chr11:63718553 | T | A | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.200-149T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63718553 | |||||||
| chr11:63718555 | A | C | 1 | a0002c0002t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.200-147A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 2/8 | chr11 | 63718555 | |||||||
| chr11:63721101 | A | T | 9 | a0002c0002t0001g0019 a0002c0002t0001g0033 a0002c0002t0001g0034 others(6): Show |
9 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.2530+69A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63721101 | |||||||
| chr11:63721293 | C | T | 1 | a0002c0002t0002g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2530+261C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63721293 | |||||||
| chr11:63721375 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2530+343C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63721375 | |||||||
| chr11:63721444 | G | A | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2530+412G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63721444 | |||||||
| chr11:63721491 | C | T | 1 | a0002c0002t0003g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2530+459C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63721491 | |||||||
| chr11:63721531 | C | T | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2530+499C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63721531 | |||||||
| chr11:63721574 | C | CA | 7 | a0001c0001t0001g0164 a0001c0001t0002g0133 a0002c0002t0002g0139 others(4): Show |
7 | HG01978.hp2 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2530+559dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63721574 | ||||||
| chr11:63721724 | C | G | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+692C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63721724 | |||||||
| chr11:63722132 | T | G | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+1100T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63722132 | |||||||
| chr11:63722354 | T | C | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2530+1322T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63722354 | |||||||
| chr11:63722491 | T | C | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2530+1459T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63722491 | |||||||
| chr11:63723231 | C | A | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2530+2199C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63723231 | |||||||
| chr11:63723232 | G | A | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2530+2200G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63723232 | |||||||
| chr11:63723400 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0008g0047 a0001c0001t0008g0049 others(3): Show |
6 | HG01074.hp2 HG01928.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2530+2368A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63723400 | |||||||
| chr11:63723416 | C | CT | 13 | a0001c0001t0001g0056 a0002c0002t0006g0040 a0002c0002t0006g0041 others(10): Show |
13 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.2530+2401dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63723416 | ||||||
| chr11:63723416 | CT | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0121 a0001c0001t0001g0157 others(4): Show |
7 | HG00558.hp2 HG01496.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2530+2401delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63723416 | ||||||
| chr11:63723433 | T | A | 1 | a0002c0002t0004g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2530+2401T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63723433 | |||||||
| chr11:63723778 | A | G | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2530+2746A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63723778 | |||||||
| chr11:63723796 | A | G | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2530+2764A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63723796 | |||||||
| chr11:63724129 | G | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+3097G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724129 | |||||||
| chr11:63724173 | C | CT | 43 | a0001c0001t0001g0046 a0001c0001t0001g0059 a0001c0001t0001g0066 others(40): Show |
43 | HG00099.hp2 HG00597.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2530+3168dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63724173 | ||||||
| chr11:63724173 | C | CTT | 8 | a0002c0002t0001g0033 a0002c0002t0001g0037 a0002c0002t0002g0151 others(5): Show |
8 | HG01433.hp1 HG02145.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2530+3167_2530+316 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63724173 | ||||||
| chr11:63724173 | C | CTTT | 7 | a0002c0002t0001g0020 a0002c0002t0001g0024 a0002c0002t0006g0111 others(4): Show |
7 | HG01496.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2530+3166_2530+316 others(7): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63724173 | ||||||
| chr11:63724173 | CTTTTTTT others(6): Show |
C | 2 | a0003c0003t0001g0008 a0003c0003t0001g0009 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2530+3156_2530+316 others(17): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63724173 | ||||||
| chr11:63724283 | C | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+3251C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724283 | |||||||
| chr11:63724324 | G | A | 10 | a0002c0002t0001g0138 a0002c0002t0004g0010 a0002c0002t0004g0011 others(7): Show |
10 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2530+3292G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724324 | |||||||
| chr11:63724344 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2530+3312G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724344 | |||||||
| chr11:63724364 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2530+3332T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724364 | |||||||
| chr11:63724425 | T | C | 153 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(150): Show |
153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2530+3393T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724425 | |||||||
| chr11:63724465 | G | T | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2530+3433G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724465 | |||||||
| chr11:63724484 | C | CT | 45 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0046 others(42): Show |
45 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.2530+3476dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63724484 | ||||||
| chr11:63724484 | CT | C | 12 | a0001c0001t0001g0085 a0002c0002t0001g0020 a0002c0002t0001g0023 others(9): Show |
12 | HG01496.hp1 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2530+3476delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63724484 | ||||||
| chr11:63724508 | T | TA | 12 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(9): Show |
12 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2530+3479dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63724508 | ||||||
| chr11:63724652 | C | A | 1 | a0001c0001t0001g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2530+3620C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724652 | |||||||
| chr11:63724822 | A | C | 1 | a0002c0002t0001g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2530+3790A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724822 | |||||||
| chr11:63724964 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2530+3932G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724964 | |||||||
| chr11:63724969 | T | G | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2530+3937T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63724969 | |||||||
| chr11:63725234 | A | T | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2530+4202A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725234 | |||||||
| chr11:63725257 | C | T | 3 | a0002c0002t0001g0163 a0002c0002t0002g0151 a0002c0002t0002g0154 |
3 | HG01243.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2530+4225C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725257 | |||||||
| chr11:63725338 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0083 others(2): Show |
5 | HG00642.hp1 HG01123.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2530+4306A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725338 | |||||||
| chr11:63725432 | C | CT | 19 | a0002c0002t0001g0019 a0002c0002t0001g0033 a0002c0002t0001g0034 others(16): Show |
19 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.2530+4411dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63725432 | ||||||
| chr11:63725518 | C | T | 9 | a0002c0002t0001g0019 a0002c0002t0001g0033 a0002c0002t0001g0034 others(6): Show |
9 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.2530+4486C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725518 | |||||||
| chr11:63725522 | C | A | 3 | a0002c0002t0009g0031 a0002c0002t0009g0099 a0002c0002t0009g0101 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2530+4490C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725522 | |||||||
| chr11:63725614 | A | G | 3 | a0002c0002t0004g0011 a0002c0002t0004g0016 a0002c0002t0004g0018 |
3 | HG01109.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2530+4582A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725614 | |||||||
| chr11:63725698 | C | T | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2530+4666C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725698 | |||||||
| chr11:63725741 | C | T | 1 | a0003c0003t0005g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2530+4709C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725741 | |||||||
| chr11:63725831 | G | A | 4 | a0002c0002t0001g0019 a0002c0002t0001g0034 a0002c0002t0002g0035 others(1): Show |
4 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+4799G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725831 | |||||||
| chr11:63725906 | G | A | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2530+4874G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63725906 | |||||||
| chr11:63726054 | G | GA | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+5030dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63726054 | ||||||
| chr11:63726231 | C | T | 1 | a0002c0002t0003g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2530+5199C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726231 | |||||||
| chr11:63726243 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2530+5211G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726243 | |||||||
| chr11:63726447 | G | A | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2530+5415G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726447 | |||||||
| chr11:63726538 | A | G | 3 | a0002c0002t0001g0163 a0002c0002t0002g0151 a0002c0002t0002g0154 |
3 | HG01243.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2530+5506A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726538 | |||||||
| chr11:63726586 | G | A | 1 | a0002c0002t0003g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2530+5554G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726586 | |||||||
| chr11:63726592 | A | G | 1 | a0002c0002t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2530+5560A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726592 | |||||||
| chr11:63726601 | G | A | 1 | a0002c0006t0001g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2530+5569G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726601 | |||||||
| chr11:63726603 | CT | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0084 |
2 | HG00642.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2530+5572delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726603 | |||||||
| chr11:63726796 | AG | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+5766delG | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63726796 | ||||||
| chr11:63726798 | G | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+5766G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726798 | |||||||
| chr11:63726826 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2530+5794C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726826 | |||||||
| chr11:63726860 | T | TC | 5 | a0001c0001t0002g0133 a0002c0002t0004g0010 a0002c0002t0004g0011 others(2): Show |
5 | HG02486.hp1 HG03453.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2530+5828_2530+582 others(5): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726860 | |||||||
| chr11:63726860 | T | TCA | 2 | a0002c0002t0004g0012 a0002c0002t0004g0016 |
2 | HG01109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2530+5828_2530+582 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726860 | |||||||
| chr11:63726860 | TG | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0028 |
2 | HG00323.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2530+5829delG | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726860 | |||||||
| chr11:63726861 | G | A | 7 | a0001c0001t0002g0133 a0002c0002t0004g0010 a0002c0002t0004g0011 others(4): Show |
7 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.2530+5829G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726861 | |||||||
| chr11:63726861 | G | C | 152 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2530+5829G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726861 | |||||||
| chr11:63726862 | A | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0028 |
2 | HG00323.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2530+5830A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726862 | |||||||
| chr11:63726868 | A | C | 1 | a0002c0002t0004g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2530+5836A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726868 | |||||||
| chr11:63726879 | G | C | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2530+5847G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726879 | |||||||
| chr11:63726886 | TGAGCC | T | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(90): Show |
93 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2530+5858_2530+586 others(9): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63726886 | ||||||
| chr11:63726891 | C | T | 35 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(32): Show |
35 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.2530+5859C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726891 | |||||||
| chr11:63726991 | G | C | 1 | a0002c0002t0007g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2530+5959G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63726991 | |||||||
| chr11:63727481 | AAG | A | 10 | a0002c0002t0005g0095 a0003c0003t0005g0094 a0003c0003t0005g0096 others(7): Show |
10 | HG00642.hp2 HG00738.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.2530+6452_2530+645 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63727481 | ||||||
| chr11:63727715 | C | T | 13 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(10): Show |
13 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.2530+6683C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63727715 | |||||||
| chr11:63727914 | C | T | 4 | a0002c0002t0007g0002 a0002c0002t0007g0004 a0002c0002t0007g0005 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+6882C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63727914 | |||||||
| chr11:63727986 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2530+6954A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63727986 | |||||||
| chr11:63728024 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0014g0127 |
2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2530+6992A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63728024 | |||||||
| chr11:63728111 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2530+7079G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63728111 | |||||||
| chr11:63728177 | C | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2530+7145C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63728177 | |||||||
| chr11:63728685 | C | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2530+7653C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63728685 | |||||||
| chr11:63728844 | G | A | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2530+7812G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63728844 | |||||||
| chr11:63728886 | C | CA | 13 | a0002c0002t0001g0037 a0002c0002t0001g0039 a0002c0002t0001g0137 others(10): Show |
13 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.2530+7870dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63728886 | ||||||
| chr11:63728886 | CA | C | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2530+7870delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63728886 | ||||||
| chr11:63728905 | AAAAAG | A | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2530+7882_2530+788 others(9): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63728905 | ||||||
| chr11:63728912 | AAAG | A | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2530+7883_2530+788 others(7): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63728912 | ||||||
| chr11:63729090 | A | C | 1 | a0004c0004t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2530+8058A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729090 | |||||||
| chr11:63729340 | T | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(30): Show |
33 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.2530+8308T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729340 | |||||||
| chr11:63729348 | C | T | 1 | a0002c0002t0003g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2530+8316C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729348 | |||||||
| chr11:63729375 | C | A | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2530+8343C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729375 | |||||||
| chr11:63729380 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2530+8348G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729380 | |||||||
| chr11:63729436 | C | CT | 52 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0046 others(49): Show |
52 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.2530+8427dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63729436 | ||||||
| chr11:63729436 | C | CTT | 16 | a0001c0001t0001g0007 a0002c0002t0001g0020 a0002c0002t0001g0146 others(13): Show |
16 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2530+8426_2530+842 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63729436 | ||||||
| chr11:63729436 | C | CTTT | 5 | a0002c0002t0001g0030 a0002c0002t0003g0110 a0002c0002t0003g0142 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2530+8425_2530+842 others(7): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63729436 | ||||||
| chr11:63729459 | TG | T | 4 | a0001c0001t0001g0063 a0002c0002t0004g0014 a0002c0002t0004g0015 others(1): Show |
4 | HG01074.hp1 HG02717.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+8428delG | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729459 | |||||||
| chr11:63729460 | G | T | 162 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.2530+8428G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729460 | |||||||
| chr11:63729540 | C | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(90): Show |
93 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2530+8508C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729540 | |||||||
| chr11:63729568 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2530+8536G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729568 | |||||||
| chr11:63729679 | T | C | 1 | a0002c0002t0001g0160 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2530+8647T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63729679 | |||||||
| chr11:63729989 | CAG | C | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+8960_2530+896 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63729989 | ||||||
| chr11:63731075 | A | AT | 13 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(10): Show |
13 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2530+10054dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63731075 | ||||||
| chr11:63731083 | T | A | 5 | a0002c0002t0001g0102 a0002c0002t0001g0103 a0002c0006t0001g0145 others(2): Show |
5 | HG03098.hp1 HG03195.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.2530+10051T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63731083 | |||||||
| chr11:63731086 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2530+10054T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63731086 | |||||||
| chr11:63731087 | A | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+10055A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63731087 | |||||||
| chr11:63731091 | A | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+10059A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63731091 | |||||||
| chr11:63731684 | C | T | 10 | a0002c0002t0005g0095 a0003c0003t0005g0094 a0003c0003t0005g0096 others(7): Show |
10 | HG00642.hp2 HG00738.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.2530+10652C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63731684 | |||||||
| chr11:63731825 | G | C | 5 | a0002c0002t0002g0105 a0002c0002t0002g0106 a0002c0002t0002g0139 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2530+10793G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63731825 | |||||||
| chr11:63731937 | C | T | 1 | a0002c0002t0006g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2530+10905C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63731937 | |||||||
| chr11:63732395 | G | A | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2530+11363G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63732395 | |||||||
| chr11:63732495 | G | GA | 13 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(10): Show |
13 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2530+11475dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63732495 | ||||||
| chr11:63732656 | A | G | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2530+11624A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63732656 | |||||||
| chr11:63733008 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0003g0116 |
2 | HG00323.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2530+11976G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63733008 | |||||||
| chr11:63733160 | C | CA | 15 | a0001c0005t0001g0109 a0002c0002t0001g0102 a0002c0002t0001g0103 others(12): Show |
15 | HG00558.hp2 HG01109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.2530+12139dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63733160 | ||||||
| chr11:63733178 | G | C | 8 | a0002c0002t0003g0110 a0002c0002t0003g0142 a0002c0002t0003g0143 others(5): Show |
8 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2530+12146G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63733178 | |||||||
| chr11:63733192 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2530+12160G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63733192 | |||||||
| chr11:63733514 | T | C | 13 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(10): Show |
13 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2530+12482T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63733514 | |||||||
| chr11:63733750 | C | T | 4 | a0002c0002t0001g0102 a0002c0002t0001g0103 a0003c0003t0001g0008 others(1): Show |
4 | HG03098.hp1 HG03195.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+12718C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63733750 | |||||||
| chr11:63733751 | G | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0085 others(3): Show |
6 | HG01243.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2530+12719G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63733751 | |||||||
| chr11:63733920 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2530+12888G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63733920 | |||||||
| chr11:63733964 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2530+12932A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63733964 | |||||||
| chr11:63734018 | A | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0010g0064 |
3 | HG01169.hp2 HG01255.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2530+12986A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63734018 | |||||||
| chr11:63734111 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0089 |
2 | HG01192.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2530+13079T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63734111 | |||||||
| chr11:63734360 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2530+13328T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63734360 | |||||||
| chr11:63734640 | G | A | 4 | a0002c0002t0007g0002 a0002c0002t0007g0004 a0002c0002t0007g0005 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+13608G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63734640 | |||||||
| chr11:63734734 | A | AAC | 4 | a0002c0002t0001g0150 a0002c0002t0003g0147 a0002c0002t0007g0005 others(1): Show |
4 | HG00738.hp1 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+13749_2530+13 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | A | AACAC | 10 | a0002c0002t0002g0035 a0002c0002t0002g0139 a0002c0002t0003g0110 others(7): Show |
10 | HG00738.hp2 HG02622.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.2530+13747_2530+13 others(10): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | A | AACACAC | 14 | a0002c0002t0001g0033 a0002c0002t0001g0037 a0002c0002t0001g0038 others(11): Show |
14 | HG01109.hp1 HG01433.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2530+13745_2530+13 others(12): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | A | AACACACA others(1): Show |
5 | a0002c0002t0001g0039 a0002c0002t0001g0113 a0002c0002t0001g0149 others(2): Show |
5 | HG01109.hp2 HG02071.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2530+13743_2530+13 others(14): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | A | AACACACA others(3): Show |
1 | a0002c0002t0017g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2530+13741_2530+13 others(16): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | A | AACACACA others(5): Show |
1 | a0002c0002t0001g0137 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2530+13739_2530+13 others(18): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | A | AACACACA others(9): Show |
1 | a0002c0002t0004g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2530+13735_2530+13 others(22): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | A | AACACACA others(13): Show |
1 | a0002c0002t0004g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2530+13731_2530+13 others(26): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | AAC | A | 20 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0055 others(17): Show |
20 | HG00280.hp2 HG00558.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2530+13749_2530+13 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | AACAC | A | 18 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0059 others(15): Show |
18 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.2530+13747_2530+13 others(10): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | AACACAC | A | 4 | a0002c0002t0001g0146 a0003c0003t0005g0096 a0003c0003t0005g0135 others(1): Show |
4 | HG02683.hp2 HG03471.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.2530+13745_2530+13 others(12): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | AACACACA others(3): Show |
A | 4 | a0002c0002t0001g0019 a0002c0002t0001g0024 a0002c0002t0001g0030 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+13741_2530+13 others(16): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | AACACACA others(5): Show |
A | 5 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0009g0031 others(2): Show |
5 | HG01496.hp1 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2530+13739_2530+13 others(18): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734734 | AACACACA others(9): Show |
A | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2530+13735_2530+13 others(22): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734734 | ||||||
| chr11:63734779 | A | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0083 |
2 | HG01952.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2530+13747A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63734779 | |||||||
| chr11:63734781 | A | ACACACC | 2 | a0001c0001t0001g0029 a0001c0001t0003g0116 |
2 | HG01433.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2530+13750_2530+13 others(12): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734781 | ||||||
| chr11:63734781 | A | ACACC | 9 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0080 others(6): Show |
9 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.2530+13750_2530+13 others(10): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734781 | ||||||
| chr11:63734781 | A | ACC | 14 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0051 others(11): Show |
14 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2530+13750_2530+13 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63734781 | ||||||
| chr11:63734781 | A | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(64): Show |
67 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.2530+13749A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63734781 | |||||||
| chr11:63734811 | T | C | 3 | a0002c0002t0009g0031 a0002c0002t0009g0099 a0002c0002t0009g0101 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2530+13779T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63734811 | |||||||
| chr11:63735028 | TA | T | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2530+14006delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735028 | ||||||
| chr11:63735338 | A | G | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530+14306A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63735338 | |||||||
| chr11:63735550 | T | TCTCTCTC others(12): Show |
1 | a0002c0002t0002g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2531-14441_2531-14 others(25): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63735550 | |||||||
| chr11:63735550 | T | TTC | 12 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0121 others(9): Show |
12 | HG00642.hp2 HG01433.hp1 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.2531-14391_2531-14 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTC | 4 | a0002c0002t0001g0020 a0002c0002t0001g0039 a0002c0002t0007g0005 others(1): Show |
4 | HG01496.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-14393_2531-14 others(10): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTC | 11 | a0001c0001t0001g0065 a0001c0001t0001g0072 a0001c0001t0001g0084 others(8): Show |
11 | HG00280.hp2 HG00642.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.2531-14395_2531-14 others(12): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(1): Show |
13 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0062 others(10): Show |
13 | HG01169.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2531-14397_2531-14 others(14): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(3): Show |
21 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0046 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.2531-14399_2531-14 others(16): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(5): Show |
18 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): Show |
18 | HG00323.hp2 HG00621.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2531-14401_2531-14 others(18): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(7): Show |
16 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0056 others(13): Show |
16 | HG00099.hp2 HG01074.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.2531-14403_2531-14 others(20): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(9): Show |
12 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0078 others(9): Show |
12 | HG00597.hp1 HG00738.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2531-14405_2531-14 others(22): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(11): Show |
13 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0076 others(10): Show |
13 | HG00099.hp1 HG00558.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.2531-14407_2531-14 others(24): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(13): Show |
5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0002c0002t0002g0140 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2531-14409_2531-14 others(26): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(15): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0157 a0004c0004t0001g0168 |
3 | HG02630.hp2 HG02735.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2531-14411_2531-14 others(28): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(17): Show |
3 | a0001c0001t0001g0052 a0002c0002t0001g0019 a0003c0003t0005g0135 |
3 | HG04184.hp2 HG06807.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2531-14413_2531-14 others(30): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(19): Show |
1 | a0001c0001t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2531-14415_2531-14 others(32): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(21): Show |
1 | a0003c0003t0001g0008 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2531-14417_2531-14 others(34): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | T | TTCTCTCT others(25): Show |
1 | a0002c0002t0002g0105 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2531-14421_2531-14 others(38): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | TTCTC | T | 3 | a0001c0001t0001g0079 a0001c0001t0003g0117 a0002c0002t0003g0107 |
3 | HG03098.hp2 NA19000.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2531-14393_2531-14 others(10): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735550 | TTCTCTC | T | 4 | a0002c0002t0001g0033 a0002c0002t0001g0138 a0002c0002t0001g0149 others(1): Show |
4 | HG01109.hp2 HG02735.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2531-14395_2531-14 others(12): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735550 | ||||||
| chr11:63735561 | T | TCTCTCTC others(3): Show |
1 | a0001c0001t0001g0055 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2531-14421_2531-14 others(16): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735561 | ||||||
| chr11:63735567 | T | TCTCTCTC others(15): Show |
1 | a0001c0001t0001g0006 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2531-14403_2531-14 others(28): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735567 | ||||||
| chr11:63735584 | CTCTCTCT others(11): Show |
C | 3 | a0002c0002t0004g0011 a0002c0002t0004g0016 a0002c0002t0004g0018 |
3 | HG01109.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2531-14403_2531-14 others(24): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735584 | ||||||
| chr11:63735590 | CTCTCTCT others(5): Show |
C | 2 | a0002c0002t0004g0014 a0002c0002t0004g0015 |
2 | HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2531-14397_2531-14 others(18): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735590 | ||||||
| chr11:63735596 | CTCTCT | C | 2 | a0002c0002t0001g0137 a0002c0002t0007g0032 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2531-14393_2531-14 others(11): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63735596 | ||||||
| chr11:63735601 | T | TCTCTCTC others(2): Show |
3 | a0001c0001t0001g0057 a0002c0002t0005g0095 a0003c0003t0005g0096 |
3 | HG02683.hp2 HG03017.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2531-14390_2531-14 others(15): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63735601 | |||||||
| chr11:63735601 | T | TCTCTCTC others(8): Show |
2 | a0001c0001t0001g0122 a0001c0001t0001g0156 |
2 | HG00597.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2531-14390_2531-14 others(21): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63735601 | |||||||
| chr11:63735601 | T | TCTCTCTC others(14): Show |
2 | a0002c0002t0002g0114 a0002c0002t0006g0158 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2531-14390_2531-14 others(27): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63735601 | |||||||
| chr11:63735601 | T | TCTCTCTC others(18): Show |
1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2531-14390_2531-14 others(31): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63735601 | |||||||
| chr11:63735602 | T | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0065 a0002c0002t0004g0010 others(3): Show |
6 | HG00280.hp2 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2531-14389T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63735602 | |||||||
| chr11:63735630 | A | G | 2 | a0003c0003t0001g0008 a0003c0003t0001g0009 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2531-14361A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63735630 | |||||||
| chr11:63735795 | G | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2531-14196G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63735795 | |||||||
| chr11:63736303 | ATC | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-13686_2531-13 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63736303 | ||||||
| chr11:63736413 | C | T | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2531-13578C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63736413 | |||||||
| chr11:63736469 | C | T | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2531-13522C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63736469 | |||||||
| chr11:63736530 | T | TA | 2 | a0002c0002t0007g0032 a0002c0002t0007g0112 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2531-13460dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63736530 | ||||||
| chr11:63736580 | C | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-13411C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63736580 | |||||||
| chr11:63736619 | C | T | 3 | a0002c0002t0006g0041 a0002c0002t0006g0042 a0002c0002t0006g0158 |
3 | HG02145.hp2 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2531-13372C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63736619 | |||||||
| chr11:63736695 | A | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2531-13296A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63736695 | |||||||
| chr11:63736973 | C | CT | 13 | a0002c0002t0005g0095 a0002c0002t0006g0115 a0002c0006t0001g0145 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2531-13002dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63736973 | ||||||
| chr11:63736988 | T | C | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-13003T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63736988 | |||||||
| chr11:63736989 | T | C | 13 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(10): Show |
13 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2531-13002T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63736989 | |||||||
| chr11:63737017 | T | C | 8 | a0002c0002t0003g0110 a0002c0002t0003g0142 a0002c0002t0003g0143 others(5): Show |
8 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2531-12974T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63737017 | |||||||
| chr11:63737122 | C | G | 3 | a0002c0002t0009g0031 a0002c0002t0009g0099 a0002c0002t0009g0101 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2531-12869C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63737122 | |||||||
| chr11:63737174 | G | A | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2531-12817G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63737174 | |||||||
| chr11:63737177 | G | A | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2531-12814G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63737177 | |||||||
| chr11:63737290 | G | A | 1 | a0001c0001t0013g0129 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2531-12701G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63737290 | |||||||
| chr11:63737342 | T | C | 8 | a0002c0002t0003g0110 a0002c0002t0003g0142 a0002c0002t0003g0143 others(5): Show |
8 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2531-12649T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63737342 | |||||||
| chr11:63737533 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0122 |
2 | HG00597.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.2531-12458C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63737533 | |||||||
| chr11:63737620 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2531-12371A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63737620 | |||||||
| chr11:63737956 | G | A | 2 | a0002c0002t0002g0035 a0002c0002t0002g0036 |
2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2531-12035G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63737956 | |||||||
| chr11:63738044 | C | T | 49 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(46): Show |
49 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.2531-11947C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63738044 | |||||||
| chr11:63738109 | A | G | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-11882A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63738109 | |||||||
| chr11:63738355 | A | C | 9 | a0002c0002t0001g0019 a0002c0002t0001g0033 a0002c0002t0001g0034 others(6): Show |
9 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.2531-11636A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63738355 | |||||||
| chr11:63738624 | C | T | 1 | a0003c0003t0015g0093 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2531-11367C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63738624 | |||||||
| chr11:63738632 | T | TA | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(100): Show |
103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.2531-11342dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63738632 | ||||||
| chr11:63738714 | A | G | 3 | a0002c0002t0009g0031 a0002c0002t0009g0099 a0002c0002t0009g0101 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2531-11277A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63738714 | |||||||
| chr11:63738727 | C | G | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2531-11264C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63738727 | |||||||
| chr11:63738882 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2531-11109A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63738882 | |||||||
| chr11:63738927 | T | C | 3 | a0002c0002t0009g0031 a0002c0002t0009g0099 a0002c0002t0009g0101 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2531-11064T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63738927 | |||||||
| chr11:63739698 | C | A | 3 | a0002c0002t0009g0031 a0002c0002t0009g0099 a0002c0002t0009g0101 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2531-10293C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63739698 | |||||||
| chr11:63739702 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2531-10289C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63739702 | |||||||
| chr11:63740124 | C | T | 1 | a0002c0002t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2531-9867C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63740124 | |||||||
| chr11:63740446 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2531-9545T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63740446 | |||||||
| chr11:63740448 | A | AT | 21 | a0001c0001t0001g0084 a0001c0001t0001g0121 a0001c0001t0001g0157 others(18): Show |
21 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.2531-9521dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63740448 | ||||||
| chr11:63740448 | A | ATT | 6 | a0001c0001t0001g0029 a0002c0002t0004g0011 a0002c0002t0004g0013 others(3): Show |
6 | HG01433.hp2 HG02622.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2531-9522_2531-952 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63740448 | ||||||
| chr11:63740448 | AT | A | 8 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(5): Show |
8 | HG01109.hp2 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2531-9521delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63740448 | ||||||
| chr11:63740478 | T | C | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-9513T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63740478 | |||||||
| chr11:63740567 | G | C | 1 | a0002c0002t0004g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2531-9424G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63740567 | |||||||
| chr11:63740617 | G | C | 13 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(10): Show |
13 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2531-9374G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63740617 | |||||||
| chr11:63740862 | T | C | 36 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(33): Show |
36 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.2531-9129T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63740862 | |||||||
| chr11:63741025 | G | A | 1 | a0003c0003t0015g0093 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2531-8966G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63741025 | |||||||
| chr11:63741200 | TA | T | 3 | a0003c0003t0005g0096 a0003c0003t0005g0097 a0003c0003t0005g0136 |
3 | HG00642.hp2 HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2531-8790delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63741200 | |||||||
| chr11:63741204 | TA | T | 6 | a0002c0002t0001g0103 a0002c0002t0002g0151 a0002c0002t0005g0095 others(3): Show |
6 | HG00738.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2531-8786delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63741204 | |||||||
| chr11:63741205 | A | T | 16 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0045 others(13): Show |
16 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.2531-8786A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63741205 | |||||||
| chr11:63741208 | TA | T | 13 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(10): Show |
13 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.2531-8782delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63741208 | |||||||
| chr11:63741209 | A | T | 59 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0044 others(56): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.2531-8782A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63741209 | |||||||
| chr11:63741213 | A | T | 161 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.2531-8778A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63741213 | |||||||
| chr11:63741384 | TAG | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2531-8602_2531-860 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63741384 | ||||||
| chr11:63741428 | C | CTGACCT | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2531-8561_2531-855 others(10): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63741428 | ||||||
| chr11:63741448 | C | T | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2531-8543C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63741448 | |||||||
| chr11:63741505 | A | AT | 8 | a0001c0001t0001g0061 a0001c0001t0001g0090 a0002c0002t0001g0102 others(5): Show |
8 | HG01192.hp1 HG01928.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2531-8474dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63741505 | ||||||
| chr11:63741637 | CT | C | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2531-8352delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63741637 | ||||||
| chr11:63741943 | C | T | 1 | a0002c0002t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2531-8048C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63741943 | |||||||
| chr11:63742064 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2531-7927C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63742064 | |||||||
| chr11:63742082 | C | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-7909C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63742082 | |||||||
| chr11:63742231 | G | A | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2531-7760G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63742231 | |||||||
| chr11:63742393 | C | A | 1 | a0002c0002t0001g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2531-7598C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63742393 | |||||||
| chr11:63742576 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2531-7415C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63742576 | |||||||
| chr11:63742659 | A | G | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-7332A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63742659 | |||||||
| chr11:63742869 | TTTTG | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0130 a0001c0001t0010g0064 others(1): Show |
4 | HG01255.hp1 HG01255.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-7098_2531-709 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63742869 | ||||||
| chr11:63742927 | T | C | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2531-7064T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63742927 | |||||||
| chr11:63742941 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2531-7050C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63742941 | |||||||
| chr11:63743090 | G | A | 5 | a0001c0001t0001g0089 a0002c0002t0001g0020 a0002c0002t0001g0023 others(2): Show |
5 | HG01192.hp2 HG01496.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2531-6901G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743090 | |||||||
| chr11:63743190 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2531-6801C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743190 | |||||||
| chr11:63743193 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2531-6798G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743193 | |||||||
| chr11:63743406 | G | A | 1 | a0002c0002t0004g0015 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2531-6585G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743406 | |||||||
| chr11:63743725 | G | A | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2531-6266G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743725 | |||||||
| chr11:63743734 | G | T | 1 | a0002c0002t0001g0034 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2531-6257G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743734 | |||||||
| chr11:63743739 | A | C | 1 | a0002c0002t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2531-6252A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743739 | |||||||
| chr11:63743749 | T | C | 1 | a0002c0002t0003g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2531-6242T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743749 | |||||||
| chr11:63743873 | G | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2531-6118G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743873 | |||||||
| chr11:63743889 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2531-6102G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63743889 | |||||||
| chr11:63744020 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0084 |
2 | HG00642.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2531-5971G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63744020 | |||||||
| chr11:63744240 | C | CA | 111 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0025 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.2531-5725dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63744240 | ||||||
| chr11:63744240 | C | CAA | 37 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0048 others(34): Show |
37 | HG00558.hp2 HG00621.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2531-5726_2531-572 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63744240 | ||||||
| chr11:63744240 | C | CAAA | 8 | a0001c0001t0001g0061 a0001c0001t0001g0090 a0002c0002t0001g0102 others(5): Show |
8 | HG01192.hp1 HG01928.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2531-5727_2531-572 others(7): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63744240 | ||||||
| chr11:63744240 | C | CAAAAAAA others(4): Show |
3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0030 |
3 | HG02258.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2531-5735_2531-572 others(15): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63744240 | ||||||
| chr11:63744354 | A | G | 5 | a0002c0002t0001g0102 a0002c0002t0001g0103 a0002c0006t0001g0145 others(2): Show |
5 | HG03098.hp1 HG03195.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.2531-5637A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63744354 | |||||||
| chr11:63744603 | A | G | 13 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(10): Show |
13 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2531-5388A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63744603 | |||||||
| chr11:63745093 | T | C | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(90): Show |
93 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2531-4898T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63745093 | |||||||
| chr11:63745115 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0003g0116 |
3 | HG00323.hp2 HG02071.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2531-4876C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63745115 | |||||||
| chr11:63745462 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2531-4529T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63745462 | |||||||
| chr11:63745463 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2531-4528C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63745463 | |||||||
| chr11:63745834 | G | A | 1 | a0003c0003t0001g0009 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2531-4157G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63745834 | |||||||
| chr11:63745973 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2531-4018G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63745973 | |||||||
| chr11:63745983 | G | C | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-4008G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63745983 | |||||||
| chr11:63746197 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2531-3794C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63746197 | |||||||
| chr11:63746258 | A | G | 2 | a0002c0002t0005g0095 a0003c0003t0005g0094 |
2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2531-3733A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63746258 | |||||||
| chr11:63746366 | A | T | 1 | a0001c0005t0001g0109 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2531-3625A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63746366 | |||||||
| chr11:63746372 | A | G | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2531-3619A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63746372 | |||||||
| chr11:63746449 | T | C | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-3542T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63746449 | |||||||
| chr11:63746463 | T | G | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-3528T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63746463 | |||||||
| chr11:63746576 | G | A | 1 | a0003c0003t0005g0136 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2531-3415G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63746576 | |||||||
| chr11:63747114 | G | C | 1 | a0002c0002t0007g0002 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2531-2877G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63747114 | |||||||
| chr11:63747292 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2531-2699T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63747292 | |||||||
| chr11:63747473 | C | T | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2531-2518C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63747473 | |||||||
| chr11:63747492 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2531-2499A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63747492 | |||||||
| chr11:63747584 | G | T | 1 | a0003c0003t0001g0009 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2531-2407G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63747584 | |||||||
| chr11:63747732 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2531-2259A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63747732 | |||||||
| chr11:63748200 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2531-1791C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63748200 | |||||||
| chr11:63748280 | A | C | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2531-1711A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63748280 | |||||||
| chr11:63748295 | C | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2531-1696C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63748295 | |||||||
| chr11:63748584 | A | G | 1 | a0002c0002t0007g0112 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2531-1407A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63748584 | |||||||
| chr11:63748644 | C | G | 1 | a0001c0001t0008g0088 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2531-1347C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63748644 | |||||||
| chr11:63748661 | C | CT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0061 others(23): Show |
26 | HG01109.hp2 HG01243.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.2531-1305dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63748661 | ||||||
| chr11:63748661 | CTTTTTTT others(6): Show |
C | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-1317_2531-130 others(17): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 63748661 | ||||||
| chr11:63749008 | A | G | 7 | a0002c0002t0006g0040 a0002c0002t0006g0041 a0002c0002t0006g0042 others(4): Show |
7 | HG02145.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2531-983A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63749008 | |||||||
| chr11:63749086 | A | C | 1 | a0001c0001t0001g0006 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2531-905A>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63749086 | |||||||
| chr11:63749332 | A | G | 1 | a0001c0001t0007g0043 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2531-659A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63749332 | |||||||
| chr11:63749353 | T | C | 2 | a0002c0002t0005g0095 a0003c0003t0005g0094 |
2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2531-638T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63749353 | |||||||
| chr11:63749373 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2531-618G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63749373 | |||||||
| chr11:63749444 | A | G | 13 | a0002c0002t0005g0095 a0002c0002t0009g0031 a0002c0002t0009g0099 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2531-547A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63749444 | |||||||
| chr11:63749527 | T | A | 1 | a0002c0002t0004g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2531-464T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63749527 | |||||||
| chr11:63749651 | C | G | 1 | a0002c0002t0007g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2531-340C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 3/8 | chr11 | 63749651 | |||||||
| chr11:63750219 | C | T | 2 | a0002c0002t0001g0024 a0002c0002t0001g0030 |
2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2738+21C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63750219 | |||||||
| chr11:63750455 | C | CT | 17 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0146 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2738+272dupT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 63750455 | ||||||
| chr11:63750673 | A | G | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2738+475A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63750673 | |||||||
| chr11:63750694 | C | T | 1 | a0002c0002t0001g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2738+496C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63750694 | |||||||
| chr11:63750723 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2738+525T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63750723 | |||||||
| chr11:63750771 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2738+573G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63750771 | |||||||
| chr11:63750878 | C | T | 1 | a0002c0002t0001g0019 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2738+680C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63750878 | |||||||
| chr11:63750978 | C | T | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2738+780C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63750978 | |||||||
| chr11:63751223 | G | A | 5 | a0002c0002t0003g0110 a0002c0002t0003g0142 a0002c0002t0003g0147 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2738+1025G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63751223 | |||||||
| chr11:63751255 | C | G | 1 | a0002c0002t0007g0112 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2738+1057C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63751255 | |||||||
| chr11:63751422 | C | T | 2 | a0003c0003t0001g0008 a0003c0003t0001g0009 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2739-1085C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63751422 | |||||||
| chr11:63751519 | A | G | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2739-988A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63751519 | |||||||
| chr11:63751710 | G | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2739-797G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63751710 | |||||||
| chr11:63751730 | G | A | 1 | a0002c0002t0007g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2739-777G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63751730 | |||||||
| chr11:63751848 | C | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2739-659C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63751848 | |||||||
| chr11:63751859 | G | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2739-648G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63751859 | |||||||
| chr11:63752169 | TA | T | 34 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0054 others(31): Show |
34 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.2739-322delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 63752169 | ||||||
| chr11:63752169 | TAA | T | 14 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(11): Show |
14 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2739-323_2739-322d others(4): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 63752169 | ||||||
| chr11:63752455 | A | G | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2739-52A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 4/8 | chr11 | 63752455 | |||||||
| chr11:63752659 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0007g0043 |
2 | HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2877+14G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 5/8 | chr11 | 63752659 | |||||||
| chr11:63752893 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0092 others(1): Show |
4 | HG00323.hp2 HG00621.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2878-176C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 5/8 | chr11 | 63752893 | |||||||
| chr11:63752896 | C | T | 1 | a0002c0002t0001g0020 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2878-173C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 5/8 | chr11 | 63752896 | |||||||
| chr11:63753734 | A | T | 2 | a0002c0002t0003g0148 a0002c0002t0003g0152 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2994+26A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63753734 | |||||||
| chr11:63754107 | T | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+399T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754107 | |||||||
| chr11:63754368 | A | G | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+660A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754368 | |||||||
| chr11:63754439 | G | A | 1 | a0002c0002t0002g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2994+731G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754439 | |||||||
| chr11:63754496 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2994+788C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754496 | |||||||
| chr11:63754662 | T | A | 1 | a0002c0002t0007g0112 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2994+954T>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754662 | |||||||
| chr11:63754699 | C | CA | 9 | a0002c0002t0002g0106 a0002c0002t0002g0140 a0002c0002t0003g0107 others(6): Show |
9 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2994+1010dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63754699 | ||||||
| chr11:63754699 | CA | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.2994+1010delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63754699 | ||||||
| chr11:63754699 | CAA | C | 12 | a0001c0001t0001g0085 a0002c0002t0005g0095 a0002c0002t0009g0031 others(9): Show |
12 | HG00642.hp2 HG02622.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.2994+1009_2994+101 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63754699 | ||||||
| chr11:63754712 | A | G | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2994+1004A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754712 | |||||||
| chr11:63754715 | A | G | 2 | a0002c0002t0002g0151 a0002c0002t0002g0154 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2994+1007A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754715 | |||||||
| chr11:63754796 | G | A | 1 | a0002c0002t0001g0162 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2994+1088G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754796 | |||||||
| chr11:63754812 | A | G | 2 | a0002c0002t0002g0035 a0002c0002t0002g0036 |
2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2994+1104A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754812 | |||||||
| chr11:63754859 | T | C | 14 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0082 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.2994+1151T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754859 | |||||||
| chr11:63754884 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2994+1176C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754884 | |||||||
| chr11:63754925 | C | CA | 18 | a0002c0002t0001g0102 a0002c0002t0001g0103 a0002c0002t0001g0137 others(15): Show |
18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2995-1168dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63754925 | ||||||
| chr11:63754925 | C | CAA | 21 | a0001c0001t0001g0121 a0002c0002t0001g0033 a0002c0002t0001g0037 others(18): Show |
21 | HG01433.hp1 HG02071.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.2995-1169_2995-116 others(6): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63754925 | ||||||
| chr11:63754925 | C | CAAA | 94 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2995-1170_2995-116 others(7): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63754925 | ||||||
| chr11:63754925 | C | CAAAA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0072 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2995-1171_2995-116 others(8): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63754925 | ||||||
| chr11:63754925 | CAAA | C | 9 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2995-1170_2995-116 others(7): Show |
RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63754925 | ||||||
| chr11:63754971 | C | G | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2995-1141C>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63754971 | |||||||
| chr11:63755185 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2995-927T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63755185 | |||||||
| chr11:63755310 | G | A | 2 | a0002c0002t0004g0010 a0002c0002t0004g0012 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2995-802G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63755310 | |||||||
| chr11:63755638 | C | A | 2 | a0003c0003t0001g0008 a0003c0003t0001g0009 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2995-474C>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63755638 | |||||||
| chr11:63755651 | C | CA | 59 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0029 others(56): Show |
59 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.2995-435dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63755651 | ||||||
| chr11:63755651 | CA | C | 22 | a0001c0001t0001g0065 a0002c0002t0001g0023 a0002c0002t0001g0102 others(19): Show |
22 | HG00280.hp2 HG01109.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.2995-435delA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63755651 | ||||||
| chr11:63755776 | G | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2995-336G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63755776 | |||||||
| chr11:63755852 | G | A | 1 | a0002c0002t0001g0162 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2995-260G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63755852 | |||||||
| chr11:63755884 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2995-228G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | chr11 | 63755884 | |||||||
| chr11:63755956 | C | CA | 19 | a0001c0001t0001g0089 a0001c0001t0002g0133 a0001c0001t0008g0047 others(16): Show |
19 | HG01109.hp1 HG01192.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.2995-142dupA | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 63755956 | ||||||
| chr11:63756279 | A | T | 4 | a0002c0002t0007g0002 a0002c0002t0007g0004 a0002c0002t0007g0005 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3053+109A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63756279 | |||||||
| chr11:63756366 | C | T | 35 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(32): Show |
35 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.3053+196C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63756366 | |||||||
| chr11:63756760 | A | G | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.3053+590A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63756760 | |||||||
| chr11:63756815 | A | G | 1 | a0002c0002t0002g0105 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3053+645A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63756815 | |||||||
| chr11:63756830 | G | A | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3053+660G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63756830 | |||||||
| chr11:63756907 | G | T | 3 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0017 |
3 | HG02717.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3053+737G>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63756907 | |||||||
| chr11:63756920 | A | T | 1 | a0002c0002t0003g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3053+750A>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63756920 | |||||||
| chr11:63757301 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3054-855T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757301 | |||||||
| chr11:63757304 | C | T | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3054-852C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757304 | |||||||
| chr11:63757350 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3054-806T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757350 | |||||||
| chr11:63757355 | T | C | 1 | a0004c0004t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3054-801T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757355 | |||||||
| chr11:63757438 | G | A | 2 | a0003c0003t0005g0096 a0003c0003t0005g0136 |
2 | HG00642.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.3054-718G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757438 | |||||||
| chr11:63757501 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3054-655C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757501 | |||||||
| chr11:63757506 | A | G | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.3054-650A>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757506 | |||||||
| chr11:63757653 | T | C | 6 | a0002c0002t0004g0010 a0002c0002t0004g0011 a0002c0002t0004g0012 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.3054-503T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757653 | |||||||
| chr11:63757722 | CT | C | 95 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(92): Show |
95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.3054-417delT | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 63757722 | ||||||
| chr11:63757786 | G | C | 26 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(23): Show |
26 | HG00642.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.3054-370G>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757786 | |||||||
| chr11:63757846 | C | T | 1 | a0003c0003t0015g0093 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3054-310C>T | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63757846 | |||||||
| chr11:63758007 | G | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0023 a0002c0002t0001g0024 others(1): Show |
4 | HG01496.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3054-149G>A | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63758007 | |||||||
| chr11:63758130 | T | G | 5 | a0002c0002t0001g0102 a0002c0002t0001g0103 a0002c0006t0001g0145 others(2): Show |
5 | HG03098.hp1 HG03195.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.3054-26T>G | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63758130 | |||||||
| chr11:63758135 | T | C | 3 | a0002c0002t0003g0143 a0002c0002t0003g0153 a0002c0002t0016g0141 |
3 | HG02109.hp2 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3054-21T>C | RTN3 | ENSG00000133318.14 | transcript | ENST00000377819.10 | protein_coding | 8/8 | chr11 | 63758135 |