Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84816 |
|---|---|
| ensemblid | ENSG00000130347.13 |
| hgncid | 18647 |
| symbol | RTN4IP1 |
| name | reticulon 4 interacting protein 1 |
| refseq_nuc | NM_032730.5 |
| refseq_prot | NP_116119.2 |
| ensembl_nuc | ENST00000369063.8 |
| ensembl_prot | ENSP00000358059.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 106570771 |
| end | 106629498 |
| strand | - |
| ver | v1.2 |
| region | chr6:106570771-106629498 |
| region5000 | chr6:106565771-106634498 |
| regionname0 | RTN4IP1_chr6_106570771_106629498 |
| regionname5000 | RTN4IP1_chr6_106565771_106634498 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 396 | 391 | 90 | 70 | 181 | 14 | 34 | 141 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0002 | 0/0 | 396 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0003 | 0/0 | 396 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0004 | 0/0 | 396 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0005 | 0/0 | 396 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1191 | 182 | 27 | 37 | 76 | 11 | 29 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0002 | 0/0 | 1191 | 78 | 12 | 19 | 43 | 2 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0003 | 0/0 | 1191 | 67 | 30 | 6 | 27 | 1 | 3 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0004 | 0/0 | 1191 | 56 | 14 | 8 | 34 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0005 | 0/0 | 1191 | 5 | 5 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0006 | 0/0 | 1191 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0007 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0008 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0009 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0010 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0011 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| c0012 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1703 | 133 | 25 | 20 | 68 | 7 | 13 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0002 | 1/1 | 1703 | 70 | 12 | 18 | 17 | 6 | 15 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0003 | 0/0 | 1701 | 56 | 14 | 8 | 34 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0004 | 0/0 | 1703 | 56 | 20 | 6 | 26 | 1 | 3 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0005 | 0/0 | 1704 | 38 | 0 | 7 | 31 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0006 | 0/0 | 1703 | 11 | 1 | 5 | 0 | 0 | 5 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0007 | 0/0 | 1703 | 9 | 9 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0008 | 0/0 | 1703 | 5 | 0 | 3 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0009 | 0/0 | 1701 | 5 | 5 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0010 | 0/0 | 1700 | 4 | 1 | 3 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0011 | 0/0 | 1703 | 3 | 3 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0012 | 0/0 | 1704 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0013 | 0/0 | 1703 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0014 | 0/0 | 1703 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0015 | 0/0 | 1703 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| t0016 | 0/0 | 1703 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1191 | 182 | 27 | 37 | 76 | 11 | 29 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0002 | 0/0 | 1191 | 78 | 12 | 19 | 43 | 2 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0003 | 0/0 | 1191 | 67 | 30 | 6 | 27 | 1 | 3 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0004 | 0/0 | 1191 | 56 | 14 | 8 | 34 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0005 | 0/0 | 1191 | 5 | 5 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0008 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0009 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0011 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0002c0006 | 0/0 | 1191 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0003c0012 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0004c0007 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0005c0010 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2893 | 95 | 12 | 11 | 56 | 5 | 11 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0001t0002 | 1/1 | 2893 | 69 | 11 | 18 | 17 | 6 | 15 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0001t0006 | 0/0 | 2893 | 9 | 1 | 5 | 0 | 0 | 3 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0001t0008 | 0/0 | 2893 | 5 | 0 | 3 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0001t0011 | 0/0 | 2893 | 3 | 3 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0001t0015 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0002t0001 | 0/0 | 2893 | 36 | 11 | 9 | 12 | 2 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0002t0005 | 0/0 | 2894 | 38 | 0 | 7 | 31 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0002t0010 | 0/0 | 2890 | 4 | 1 | 3 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0003t0004 | 0/0 | 2893 | 55 | 20 | 6 | 25 | 1 | 3 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0003t0007 | 0/0 | 2893 | 8 | 8 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0003t0012 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0003t0014 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0003t0016 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0004t0003 | 0/0 | 2891 | 56 | 14 | 8 | 34 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0005t0009 | 0/0 | 2891 | 5 | 5 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0008t0001 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0009t0007 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0001c0011t0004 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0002c0006t0006 | 0/0 | 2893 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0003c0012t0002 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0004c0007t0001 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| a0005c0010t0013 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | copy fasta | chr6 | 106565771 | 106634498 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0006g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0006g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0006g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0006g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0006g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0006g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0006g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0006g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0006g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0008g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0011g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0001t0015g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0010g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0010g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0010g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0002t0010g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0012g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0012g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0003t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0004t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0005t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0008t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0009t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0001c0011t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0002c0006t0006g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0002c0006t0006g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0003c0012t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0004c0007t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| a0005c0010t0013g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | GBR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | GBR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | FIN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00280 | hp2 | a0001 | c0003 | t0004 | g0214 | EUR | FIN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | FIN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0090 | EUR | FIN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00408 | hp1 | a0001 | c0002 | t0005 | g0346 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00423 | hp1 | a0001 | c0002 | t0005 | g0352 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00423 | hp2 | a0001 | c0004 | t0003 | g0102 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00544 | hp1 | a0001 | c0001 | t0008 | g0042 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00544 | hp2 | a0001 | c0004 | t0003 | g0106 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00558 | hp1 | a0001 | c0002 | t0005 | g0332 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00597 | hp2 | a0001 | c0002 | t0005 | g0357 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00609 | hp1 | a0001 | c0002 | t0005 | g0339 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00609 | hp2 | a0001 | c0004 | t0003 | g0100 | EAS | CHS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00639 | hp2 | a0001 | c0003 | t0004 | g0217 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0371 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00733 | hp1 | a0001 | c0002 | t0010 | g0359 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0367 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0368 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0089 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0365 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01106 | hp2 | a0001 | c0003 | t0004 | g0218 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0043 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0044 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01175 | hp1 | a0001 | c0004 | t0003 | g0097 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0362 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01192 | hp1 | a0001 | c0004 | t0003 | g0128 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01192 | hp2 | a0001 | c0003 | t0004 | g0221 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01243 | hp1 | a0001 | c0002 | t0010 | g0360 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01255 | hp1 | a0001 | c0003 | t0004 | g0216 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01255 | hp2 | a0001 | c0004 | t0003 | g0129 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01257 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01258 | hp2 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01358 | hp1 | a0001 | c0002 | t0005 | g0001 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01361 | hp1 | a0001 | c0003 | t0004 | g0173 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01496 | hp2 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | IBS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0163 | EUR | IBS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | IBS | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01884 | hp1 | a0001 | c0004 | t0003 | g0099 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0205 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01891 | hp1 | a0001 | c0003 | t0004 | g0228 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01891 | hp2 | a0001 | c0005 | t0009 | g0137 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0324 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01943 | hp1 | a0001 | c0002 | t0005 | g0337 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01952 | hp1 | a0001 | c0002 | t0005 | g0325 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01952 | hp2 | a0001 | c0002 | t0010 | g0358 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01981 | hp2 | a0001 | c0004 | t0003 | g0127 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG01993 | hp2 | a0001 | c0002 | t0005 | g0001 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02004 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02004 | hp2 | a0001 | c0002 | t0005 | g0001 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0019 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02027 | hp2 | a0001 | c0004 | t0003 | g0103 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02055 | hp1 | a0001 | c0003 | t0004 | g0223 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02055 | hp2 | a0001 | c0004 | t0003 | g0101 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02056 | hp1 | a0001 | c0004 | t0003 | g0121 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02074 | hp1 | a0001 | c0002 | t0005 | g0343 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02074 | hp2 | a0001 | c0003 | t0004 | g0182 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02083 | hp2 | a0001 | c0004 | t0003 | g0119 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02132 | hp1 | a0001 | c0002 | t0005 | g0323 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02132 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02135 | hp2 | a0001 | c0003 | t0004 | g0171 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02145 | hp1 | a0001 | c0004 | t0003 | g0126 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02148 | hp2 | a0001 | c0003 | t0004 | g0166 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CDX | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02257 | hp1 | a0001 | c0003 | t0007 | g0150 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0363 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02273 | hp1 | a0001 | c0002 | t0005 | g0333 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02280 | hp1 | a0001 | c0003 | t0004 | g0210 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02280 | hp2 | a0001 | c0004 | t0003 | g0139 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0187 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02451 | hp2 | a0001 | c0003 | t0004 | g0168 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | KHV | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0227 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02615 | hp1 | a0001 | c0004 | t0003 | g0123 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02615 | hp2 | a0001 | c0005 | t0009 | g0095 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02622 | hp1 | a0001 | c0004 | t0003 | g0133 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02630 | hp1 | a0001 | c0004 | t0003 | g0134 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02647 | hp1 | a0001 | c0003 | t0007 | g0146 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02683 | hp1 | a0001 | c0003 | t0004 | g0157 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0364 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0199 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02717 | hp2 | a0001 | c0005 | t0009 | g0138 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02723 | hp1 | a0001 | c0004 | t0003 | g0136 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02809 | hp1 | a0001 | c0003 | t0004 | g0226 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02809 | hp2 | a0001 | c0003 | t0004 | g0206 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02818 | hp1 | a0001 | c0003 | t0007 | g0147 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02818 | hp2 | a0001 | c0003 | t0004 | g0179 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02895 | hp2 | a0001 | c0003 | t0004 | g0181 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02897 | hp1 | a0001 | c0003 | t0004 | g0180 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02897 | hp2 | a0001 | c0003 | t0007 | g0145 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0021 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02965 | hp1 | a0001 | c0005 | t0009 | g0131 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02965 | hp2 | a0001 | c0004 | t0003 | g0135 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02970 | hp2 | a0001 | c0003 | t0004 | g0229 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0153 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03098 | hp1 | a0001 | c0003 | t0007 | g0144 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03130 | hp2 | a0001 | c0003 | t0004 | g0209 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03139 | hp1 | a0001 | c0003 | t0004 | g0015 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03139 | hp2 | a0001 | c0004 | t0003 | g0093 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03209 | hp2 | a0003 | c0012 | t0002 | g0091 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03225 | hp2 | a0001 | c0003 | t0007 | g0149 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03453 | hp2 | a0001 | c0003 | t0007 | g0151 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03486 | hp1 | a0001 | c0004 | t0003 | g0092 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03486 | hp2 | a0001 | c0005 | t0009 | g0094 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03491 | hp2 | a0002 | c0006 | t0006 | g0369 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03492 | hp1 | a0002 | c0006 | t0006 | g0370 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03516 | hp1 | a0001 | c0003 | t0004 | g0224 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03540 | hp1 | a0001 | c0009 | t0007 | g0152 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03579 | hp2 | a0001 | c0004 | t0003 | g0124 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0366 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03927 | hp1 | a0001 | c0003 | t0004 | g0154 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0372 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0162 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04199 | hp2 | a0001 | c0003 | t0004 | g0158 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | STU | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18522 | hp1 | a0001 | c0003 | t0004 | g0208 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0015 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18612 | hp1 | a0001 | c0004 | t0003 | g0130 | EAS | CHB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18747 | hp1 | a0001 | c0003 | t0004 | g0177 | EAS | CHB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18906 | hp1 | a0001 | c0003 | t0004 | g0225 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18906 | hp2 | a0001 | c0003 | t0007 | g0148 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18942 | hp1 | a0001 | c0003 | t0012 | g0356 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18942 | hp2 | a0001 | c0004 | t0003 | g0009 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18945 | hp1 | a0001 | c0003 | t0004 | g0213 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18945 | hp2 | a0001 | c0004 | t0003 | g0004 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18946 | hp1 | a0001 | c0002 | t0005 | g0327 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18946 | hp2 | a0001 | c0004 | t0003 | g0113 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18947 | hp1 | a0001 | c0004 | t0003 | g0115 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18950 | hp2 | a0001 | c0003 | t0004 | g0176 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18952 | hp1 | a0001 | c0002 | t0005 | g0353 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18954 | hp1 | a0001 | c0002 | t0005 | g0355 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18959 | hp1 | a0001 | c0004 | t0003 | g0110 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18960 | hp1 | a0001 | c0004 | t0003 | g0116 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18961 | hp1 | a0001 | c0004 | t0003 | g0122 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18963 | hp1 | a0001 | c0002 | t0005 | g0344 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18965 | hp2 | a0001 | c0004 | t0003 | g0109 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18966 | hp1 | a0001 | c0003 | t0004 | g0169 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18966 | hp2 | a0001 | c0002 | t0005 | g0338 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18968 | hp1 | a0001 | c0004 | t0003 | g0118 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18968 | hp2 | a0001 | c0002 | t0005 | g0335 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18971 | hp1 | a0001 | c0002 | t0005 | g0334 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18971 | hp2 | a0001 | c0003 | t0004 | g0174 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18972 | hp2 | a0001 | c0003 | t0004 | g0170 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18973 | hp1 | a0001 | c0004 | t0003 | g0117 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18974 | hp1 | a0005 | c0010 | t0013 | g0018 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18975 | hp2 | a0001 | c0004 | t0003 | g0098 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18978 | hp1 | a0001 | c0004 | t0003 | g0108 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18979 | hp1 | a0001 | c0003 | t0004 | g0012 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18979 | hp2 | a0001 | c0002 | t0005 | g0336 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18982 | hp1 | a0001 | c0004 | t0003 | g0132 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18983 | hp2 | a0001 | c0002 | t0005 | g0354 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18985 | hp1 | a0001 | c0003 | t0004 | g0212 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18988 | hp2 | a0001 | c0002 | t0005 | g0342 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18989 | hp1 | a0001 | c0002 | t0005 | g0340 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18993 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18994 | hp1 | a0001 | c0004 | t0003 | g0105 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18995 | hp1 | a0001 | c0003 | t0004 | g0156 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18998 | hp2 | a0001 | c0002 | t0005 | g0345 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18999 | hp1 | a0001 | c0004 | t0003 | g0009 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19002 | hp2 | a0001 | c0004 | t0003 | g0114 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19004 | hp1 | a0001 | c0003 | t0004 | g0219 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19005 | hp1 | a0001 | c0004 | t0003 | g0004 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19005 | hp2 | a0001 | c0003 | t0004 | g0167 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19010 | hp1 | a0001 | c0004 | t0003 | g0111 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19010 | hp2 | a0001 | c0003 | t0004 | g0014 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19012 | hp1 | a0001 | c0003 | t0004 | g0215 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19012 | hp2 | a0001 | c0002 | t0005 | g0348 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19030 | hp1 | a0001 | c0004 | t0003 | g0096 | AFR | LWK | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19030 | hp2 | a0001 | c0003 | t0016 | g0141 | AFR | LWK | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19054 | hp1 | a0001 | c0002 | t0005 | g0329 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19055 | hp1 | a0001 | c0002 | t0005 | g0328 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19055 | hp2 | a0001 | c0004 | t0003 | g0004 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19057 | hp1 | a0001 | c0004 | t0003 | g0112 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19057 | hp2 | a0001 | c0002 | t0005 | g0331 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19058 | hp1 | a0001 | c0004 | t0003 | g0120 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19058 | hp2 | a0001 | c0003 | t0004 | g0155 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19060 | hp2 | a0001 | c0003 | t0004 | g0175 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19064 | hp1 | a0001 | c0003 | t0004 | g0012 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19065 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19066 | hp1 | a0001 | c0003 | t0004 | g0172 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19067 | hp1 | a0001 | c0011 | t0004 | g0233 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19067 | hp2 | a0001 | c0002 | t0005 | g0351 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19068 | hp1 | a0001 | c0002 | t0005 | g0347 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19068 | hp2 | a0001 | c0004 | t0003 | g0140 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19070 | hp1 | a0001 | c0003 | t0012 | g0349 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19072 | hp1 | a0001 | c0003 | t0004 | g0143 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19072 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19074 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19076 | hp2 | a0001 | c0002 | t0005 | g0350 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19078 | hp2 | a0001 | c0003 | t0004 | g0211 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19080 | hp2 | a0001 | c0002 | t0005 | g0341 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19081 | hp1 | a0001 | c0003 | t0004 | g0014 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19081 | hp2 | a0001 | c0001 | t0015 | g0068 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19082 | hp1 | a0001 | c0003 | t0004 | g0159 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19084 | hp1 | a0001 | c0004 | t0003 | g0107 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19084 | hp2 | a0001 | c0002 | t0005 | g0326 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19088 | hp1 | a0001 | c0003 | t0004 | g0142 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19089 | hp2 | a0001 | c0003 | t0004 | g0220 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19091 | hp2 | a0001 | c0002 | t0005 | g0330 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19240 | hp1 | a0001 | c0003 | t0004 | g0207 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | YRI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | TSI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | TSI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | TSI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0013 | EUR | TSI | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0006 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0178 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | USA | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| HG06807 | hp2 | a0004 | c0007 | t0001 | g0204 | AFR | USA | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18955 | hp1 | a0001 | c0004 | t0003 | g0104 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20300 | hp1 | a0001 | c0003 | t0014 | g0017 | AFR | USA | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA20300 | hp2 | a0001 | c0004 | t0003 | g0125 | AFR | USA | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA21309 | hp1 | a0001 | c0002 | t0010 | g0361 | AFR | LWK | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0008 | REF | REF | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0049 | REF | REF | RTN4IP1_chr6_106565771_106634498 | RTN4IP1 | chr6 | 106565771 | 106634498 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106572028
|
C | T | 1 | a0002 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.1159G>A | p.Ala387Thr | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1636/2893 | 1159/1191 | 387/396 | chr6 | 106572028 | ||
| chr6:106572093
|
A | G | 1 | a0004 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1094T>C | p.Val365Ala | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1571/2893 | 1094/1191 | 365/396 | chr6 | 106572093 | ||
| chr6:106628871
|
A | T | 1 | a0005 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.151T>A | p.Tyr51Asn | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 628/2893 | 151/1191 | 51/396 | chr6 | 106628871 | ||
| chr6:106628872
|
T | A | 1 | a0005 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.150A>T | p.Lys50Asn | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 627/2893 | 150/1191 | 50/396 | chr6 | 106628872 | ||
| chr6:106629017
|
T | G | 1 | a0003 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.5A>C | p.Glu2Ala | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 482/2893 | 5/1191 | 2/396 | chr6 | 106629017 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106572005
|
A | G | 5 | a0001c0003a0001c0005a0001c0009others(2): Show | 75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
synonymous_variant | LOW | c.1182T>C | p.Asn394Asn | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1659/2893 | 1182/1191 | 394/396 | chr6 | 106572005 | ||
| chr6:106602898
|
G | A | 1 | a0001c0008 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.645C>T | p.Gly215Gly | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/9 | 1122/2893 | 645/1191 | 215/396 | chr6 | 106602898 | ||
| chr6:106619285
|
G | A | 1 | a0001c0009 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.537C>T | p.Ala179Ala | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/9 | 1014/2893 | 537/1191 | 179/396 | chr6 | 106619285 | ||
| chr6:106628821
|
G | A | 2 | a0001c0004a0001c0005 | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
synonymous_variant | LOW | c.201C>T | p.Ile67Ile | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 678/2893 | 201/1191 | 67/396 | chr6 | 106628821 | ||
| chr6:106628908
|
A | T | 9 | a0001c0002a0001c0003a0001c0004others(6): Show | 211 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(208): Show |
synonymous_variant | LOW | c.114T>A | p.Pro38Pro | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 591/2893 | 114/1191 | 38/396 | chr6 | 106628908 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106570792
|
C | T | 3 | a0001c0003t0007a0001c0003t0014a0001c0009t0007 | 10 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1204G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1204 | chr6 | 106570792 | |||||
| chr6:106570799
|
A | G | 9 | a0001c0003t0004a0001c0003t0007a0001c0003t0012others(6): Show | 75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1197T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1197 | chr6 | 106570799 | |||||
| chr6:106570934
|
T | G | 1 | a0001c0001t0015 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1062A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1062 | chr6 | 106570934 | |||||
| chr6:106570964
|
G | A | 1 | a0001c0001t0011 | 3 | HG02109.hp1 HG02922.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1032C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 1032 | chr6 | 106570964 | |||||
| chr6:106571079
|
T | A | 2 | a0001c0003t0007a0001c0009t0007 | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*917A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 917 | chr6 | 106571079 | |||||
| chr6:106571287
|
A | G | 1 | a0001c0002t0010 | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*709T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 709 | chr6 | 106571287 | |||||
| chr6:106571412
|
C | T | 9 | a0001c0003t0004a0001c0003t0007a0001c0003t0012others(6): Show | 75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*584G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 584 | chr6 | 106571412 | |||||
| chr6:106571413
|
G | T | 3 | a0001c0001t0006a0001c0001t0008a0002c0006t0006 | 16 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*583C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 583 | chr6 | 106571413 | |||||
| chr6:106571760
|
A | G | 6 | a0001c0003t0004a0001c0003t0012a0001c0003t0016others(3): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*236T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 236 | chr6 | 106571760 | |||||
| chr6:106571785
|
C | T | 1 | a0001c0001t0015 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 211 | chr6 | 106571785 | |||||
| chr6:106571786
|
T | C | 9 | a0001c0003t0004a0001c0003t0007a0001c0003t0012others(6): Show | 75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*210A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 210 | chr6 | 106571786 | |||||
| chr6:106571791
|
A | G | 9 | a0001c0003t0004a0001c0003t0007a0001c0003t0012others(6): Show | 75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*205T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 9/9 | 205 | chr6 | 106571791 | |||||
| chr6:106629184
|
G | GA | 2 | a0001c0002t0005a0001c0003t0012 | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-164dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 164 | chr6 | 106629184 | |||||
| chr6:106629185
|
AAAG | A | 1 | a0001c0002t0010 | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-167_-165delCTT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 165 | chr6 | 106629185 | |||||
| chr6:106629290
|
A | G | 1 | a0001c0003t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-269T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 269 | chr6 | 106629290 | |||||
| chr6:106629303
|
AAG | A | 2 | a0001c0004t0003a0001c0005t0009 | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-284_-283delCT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 283 | chr6 | 106629303 | |||||
| chr6:106629305
|
G | A | 12 | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(9): Show | 243 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(240): Show |
5_prime_UTR_variant | MODIFIER | c.-284C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 284 | chr6 | 106629305 | |||||
| chr6:106629435
|
G | A | 2 | a0001c0001t0006a0002c0006t0006 | 11 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-414C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/9 | 414 | chr6 | 106629435 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106572119
|
G | T | 72 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(69): Show | 75 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(72): Show |
intron_variant | MODIFIER | c.1084-16C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572119 | ||||||
| chr6:106572213
|
A | G | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-110T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572213 | ||||||
| chr6:106572217
|
G | A | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-114C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572217 | ||||||
| chr6:106572314
|
C | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(277): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1084-211G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572314 | ||||||
| chr6:106572332
|
TCTC | T | 29 | a0001c0003t0004g0014a0001c0003t0004g0015a0001c0003t0004g0142others(26): Show | 31 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.1084-232_1084-230d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572332 | ||||||
| chr6:106572400
|
G | GA | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-298dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572400 | ||||||
| chr6:106572464
|
C | T | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-361G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572464 | ||||||
| chr6:106572525
|
C | G | 1 | a0001c0001t0002g0046 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1084-422G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572525 | ||||||
| chr6:106572531
|
T | C | 1 | a0001c0004t0003g0127 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1084-428A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572531 | ||||||
| chr6:106572574
|
T | A | 74 | a0001c0002t0001g0011a0001c0002t0001g0231a0001c0003t0004g0012others(71): Show | 78 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.1084-471A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572574 | ||||||
| chr6:106572596
|
G | A | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-493C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572596 | ||||||
| chr6:106572630
|
G | T | 1 | a0001c0001t0001g0253 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1084-527C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572630 | ||||||
| chr6:106572730
|
T | G | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-627A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572730 | ||||||
| chr6:106572741
|
T | C | 344 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(341): Show | 366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.1084-638A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572741 | ||||||
| chr6:106572778
|
TTTTGTTT others(4): Show |
T | 1 | a0001c0003t0016g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1084-686_1084-676d others(13): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572778 | ||||||
| chr6:106572779
|
TTTGTTTT others(3): Show |
T | 59 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(56): Show | 62 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.1084-686_1084-677d others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572779 | ||||||
| chr6:106572836
|
C | A | 2 | a0001c0002t0001g0011a0001c0002t0001g0231 | 3 | HG02257.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1084-733G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106572836 | ||||||
| chr6:106573030
|
G | T | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-927C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573030 | ||||||
| chr6:106573153
|
C | T | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-1050G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573153 | ||||||
| chr6:106573331
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0310 | 2 | NA18998.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1084-1228T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573331 | ||||||
| chr6:106573609
|
G | C | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1084-1506C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573609 | ||||||
| chr6:106573745
|
A | G | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-1642T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573745 | ||||||
| chr6:106573756
|
C | A | 1 | a0001c0004t0003g0125 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1084-1653G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573756 | ||||||
| chr6:106573768
|
G | A | 11 | a0001c0002t0001g0231a0001c0003t0007g0144a0001c0003t0007g0145others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1084-1665C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573768 | ||||||
| chr6:106573928
|
C | G | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-1825G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573928 | ||||||
| chr6:106573930
|
A | C | 2 | a0001c0002t0001g0011a0003c0012t0002g0091 | 3 | HG03209.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1084-1827T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573930 | ||||||
| chr6:106573933
|
C | T | 34 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(31): Show | 38 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1084-1830G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106573933 | ||||||
| chr6:106574082
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0279 | 2 | HG00408.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1084-1979T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574082 | ||||||
| chr6:106574147
|
T | C | 1 | a0001c0002t0010g0359 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1084-2044A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574147 | ||||||
| chr6:106574153
|
G | A | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2050C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574153 | ||||||
| chr6:106574154
|
A | C | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0257others(1): Show | 4 | HG03130.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-2051T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574154 | ||||||
| chr6:106574170
|
T | C | 368 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(365): Show | 391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.1084-2067A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574170 | ||||||
| chr6:106574246
|
A | AC | 351 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(348): Show | 374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.1084-2144dupG | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574246 | ||||||
| chr6:106574271
|
T | C | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2168A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574271 | ||||||
| chr6:106574317
|
T | C | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2214A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574317 | ||||||
| chr6:106574366
|
C | T | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2263G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574366 | ||||||
| chr6:106574443
|
C | CA | 10 | a0001c0001t0001g0240a0001c0001t0001g0314a0001c0001t0002g0067others(7): Show | 10 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-2341dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574443 | ||||||
| chr6:106574443
|
CA | C | 73 | a0001c0002t0001g0011a0001c0002t0001g0231a0001c0003t0004g0012others(70): Show | 77 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.1084-2341delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574443 | ||||||
| chr6:106574520
|
T | C | 238 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(235): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1084-2417A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574520 | ||||||
| chr6:106574585
|
T | C | 35 | a0001c0001t0001g0293a0001c0002t0001g0010a0001c0002t0001g0013others(32): Show | 37 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1084-2482A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574585 | ||||||
| chr6:106574590
|
G | T | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-2487C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574590 | ||||||
| chr6:106574611
|
C | T | 1 | a0001c0001t0006g0362 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1084-2508G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106574611 | ||||||
| chr6:106575130
|
A | C | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3027T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575130 | ||||||
| chr6:106575136
|
G | T | 2 | a0001c0004t0003g0101a0001c0004t0003g0125 | 2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1084-3033C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575136 | ||||||
| chr6:106575228
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1084-3125C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575228 | ||||||
| chr6:106575247
|
C | T | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3144G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575247 | ||||||
| chr6:106575291
|
G | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-3188C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575291 | ||||||
| chr6:106575306
|
C | T | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3203G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575306 | ||||||
| chr6:106575351
|
G | A | 10 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0365others(7): Show | 10 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-3248C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575351 | ||||||
| chr6:106575384
|
C | G | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3281G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575384 | ||||||
| chr6:106575439
|
C | T | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1084-3336G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575439 | ||||||
| chr6:106575492
|
G | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-3389C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575492 | ||||||
| chr6:106575512
|
T | C | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3409A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575512 | ||||||
| chr6:106575527
|
CCTCT | C | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3428_1084-342 others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575527 | ||||||
| chr6:106575555
|
C | A | 1 | a0001c0001t0002g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1084-3452G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575555 | ||||||
| chr6:106575651
|
C | T | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3548G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575651 | ||||||
| chr6:106575702
|
G | A | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-3599C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575702 | ||||||
| chr6:106575853
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1084-3750C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575853 | ||||||
| chr6:106575903
|
C | T | 1 | a0001c0005t0009g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1084-3800G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575903 | ||||||
| chr6:106575919
|
C | T | 1 | a0001c0001t0006g0364 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1084-3816G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575919 | ||||||
| chr6:106575987
|
T | A | 1 | a0001c0002t0005g0332 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1084-3884A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106575987 | ||||||
| chr6:106576040
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1084-3937T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576040 | ||||||
| chr6:106576272
|
A | G | 1 | a0001c0002t0005g0341 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1084-4169T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576272 | ||||||
| chr6:106576332
|
C | T | 34 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(31): Show | 38 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1084-4229G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576332 | ||||||
| chr6:106576352
|
C | A | 1 | a0001c0002t0001g0160 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1084-4249G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576352 | ||||||
| chr6:106576364
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1084-4261C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576364 | ||||||
| chr6:106576379
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1084-4276T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576379 | ||||||
| chr6:106576434
|
T | C | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1084-4331A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576434 | ||||||
| chr6:106576538
|
C | T | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-4435G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576538 | ||||||
| chr6:106576557
|
A | G | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-4454T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576557 | ||||||
| chr6:106576694
|
C | T | 34 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(31): Show | 38 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1084-4591G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576694 | ||||||
| chr6:106576695
|
G | A | 5 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(2): Show | 5 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084-4592C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576695 | ||||||
| chr6:106576706
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1084-4603G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576706 | ||||||
| chr6:106576758
|
C | T | 355 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(352): Show | 378 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.1084-4655G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576758 | ||||||
| chr6:106576891
|
C | T | 10 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(7): Show | 10 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-4788G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576891 | ||||||
| chr6:106576924
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1084-4821C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106576924 | ||||||
| chr6:106577032
|
A | G | 1 | a0001c0002t0001g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1084-4929T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577032 | ||||||
| chr6:106577069
|
G | A | 16 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(13): Show | 16 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-4966C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577069 | ||||||
| chr6:106577242
|
T | C | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5139A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577242 | ||||||
| chr6:106577306
|
T | A | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5203A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577306 | ||||||
| chr6:106577335
|
C | T | 1 | a0001c0001t0006g0365 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1084-5232G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577335 | ||||||
| chr6:106577367
|
C | G | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5264G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577367 | ||||||
| chr6:106577392
|
G | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1084-5289C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577392 | ||||||
| chr6:106577412
|
C | T | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5309G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577412 | ||||||
| chr6:106577447
|
C | CA | 20 | a0001c0001t0001g0232a0001c0001t0001g0248a0001c0001t0001g0279others(17): Show | 20 | HG00408.hp2 HG01099.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-5345dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | ||||||
| chr6:106577447
|
C | CAA | 238 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0234others(235): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1084-5346_1084-534 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | ||||||
| chr6:106577447
|
C | CAAA | 25 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0268others(22): Show | 25 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.1084-5347_1084-534 others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | ||||||
| chr6:106577447
|
C | CAAAA | 43 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0143others(40): Show | 45 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1084-5348_1084-534 others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | ||||||
| chr6:106577447
|
C | CAAAAA | 18 | a0001c0003t0004g0142a0001c0003t0004g0159a0001c0003t0004g0168others(15): Show | 18 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1084-5349_1084-534 others(9): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | ||||||
| chr6:106577447
|
CAAAA | C | 7 | a0001c0003t0004g0015a0001c0003t0004g0224a0001c0003t0004g0225others(4): Show | 8 | HG01891.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1084-5348_1084-534 others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577447 | ||||||
| chr6:106577519
|
A | C | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5416T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577519 | ||||||
| chr6:106577551
|
A | T | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1084-5448T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577551 | ||||||
| chr6:106577592
|
T | C | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-5489A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577592 | ||||||
| chr6:106577608
|
T | G | 1 | a0001c0001t0001g0312 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1084-5505A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577608 | ||||||
| chr6:106577624
|
A | G | 9 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(6): Show | 9 | HG01261.hp1 HG02602.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-5521T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577624 | ||||||
| chr6:106577754
|
G | A | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1083+5574C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577754 | ||||||
| chr6:106577798
|
G | A | 1 | a0001c0004t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1083+5530C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577798 | ||||||
| chr6:106577817
|
A | G | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1083+5511T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577817 | ||||||
| chr6:106577874
|
G | C | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1083+5454C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577874 | ||||||
| chr6:106577911
|
T | C | 62 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(59): Show | 65 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1083+5417A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106577911 | ||||||
| chr6:106578042
|
A | C | 318 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(315): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1083+5286T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578042 | ||||||
| chr6:106578141
|
T | C | 1 | a0001c0005t0009g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1083+5187A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578141 | ||||||
| chr6:106578308
|
T | G | 1 | a0001c0002t0001g0160 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1083+5020A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578308 | ||||||
| chr6:106578330
|
G | A | 7 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0257others(4): Show | 7 | HG02258.hp1 HG02717.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083+4998C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578330 | ||||||
| chr6:106578448
|
G | T | 259 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(256): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1083+4880C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578448 | ||||||
| chr6:106578555
|
A | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1083+4773T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578555 | ||||||
| chr6:106578802
|
A | G | 1 | a0001c0001t0008g0089 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1083+4526T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578802 | ||||||
| chr6:106578819
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1083+4509A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578819 | ||||||
| chr6:106578831
|
C | T | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1083+4497G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578831 | ||||||
| chr6:106578871
|
T | C | 1 | a0001c0004t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1083+4457A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578871 | ||||||
| chr6:106578914
|
C | CT | 39 | a0001c0001t0001g0293a0001c0002t0001g0010a0001c0002t0001g0013others(36): Show | 41 | HG00438.hp2 HG00738.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.1083+4413dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578914 | ||||||
| chr6:106578914
|
CT | C | 9 | a0001c0001t0001g0240a0001c0001t0001g0277a0001c0001t0001g0278others(6): Show | 10 | HG00323.hp1 HG01169.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1083+4413delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578914 | ||||||
| chr6:106578914
|
CTT | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1083+4412_1083+441 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578914 | ||||||
| chr6:106578948
|
A | G | 4 | a0001c0004t0003g0133a0001c0004t0003g0134a0001c0004t0003g0135others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+4380T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578948 | ||||||
| chr6:106578974
|
C | T | 1 | a0001c0003t0004g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1083+4354G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106578974 | ||||||
| chr6:106579158
|
C | G | 1 | a0001c0003t0004g0214 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1083+4170G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579158 | ||||||
| chr6:106579185
|
G | A | 2 | a0001c0004t0003g0104a0001c0004t0003g0110 | 2 | NA18955.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1083+4143C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579185 | ||||||
| chr6:106579296
|
C | T | 364 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(361): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1083+4032G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579296 | ||||||
| chr6:106579416
|
G | A | 2 | a0001c0001t0011g0006a0001c0001t0011g0021 | 3 | HG02109.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1083+3912C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579416 | ||||||
| chr6:106579460
|
C | G | 71 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(68): Show | 74 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.1083+3868G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579460 | ||||||
| chr6:106579535
|
T | C | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1083+3793A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579535 | ||||||
| chr6:106579606
|
A | G | 207 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(204): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1083+3722T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579606 | ||||||
| chr6:106579622
|
T | G | 112 | a0001c0002t0001g0011a0001c0002t0005g0001a0001c0002t0005g0323others(109): Show | 120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1083+3706A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579622 | ||||||
| chr6:106579682
|
T | C | 83 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(80): Show | 87 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1083+3646A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579682 | ||||||
| chr6:106579714
|
T | G | 1 | a0001c0005t0009g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1083+3614A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579714 | ||||||
| chr6:106579730
|
G | T | 1 | a0001c0001t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1083+3598C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579730 | ||||||
| chr6:106579781
|
CT | C | 9 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(6): Show | 9 | HG01099.hp1 HG01258.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+3546delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579781 | ||||||
| chr6:106579834
|
G | C | 3 | a0001c0001t0002g0025a0001c0001t0002g0055a0001c0001t0002g0056 | 3 | HG02109.hp2 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1083+3494C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579834 | ||||||
| chr6:106579964
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1083+3364G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106579964 | ||||||
| chr6:106580082
|
C | T | 1 | a0001c0004t0003g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1083+3246G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580082 | ||||||
| chr6:106580106
|
T | C | 5 | a0001c0003t0004g0168a0001c0003t0004g0207a0001c0003t0004g0208others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+3222A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580106 | ||||||
| chr6:106580109
|
A | G | 5 | a0001c0003t0004g0168a0001c0003t0004g0207a0001c0003t0004g0208others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+3219T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580109 | ||||||
| chr6:106580110
|
A | T | 1 | a0001c0002t0001g0202 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1083+3218T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580110 | ||||||
| chr6:106580146
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1083+3182C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580146 | ||||||
| chr6:106580213
|
C | CA | 40 | a0001c0001t0001g0282a0001c0001t0001g0299a0001c0001t0002g0020others(37): Show | 42 | HG00544.hp1 HG00642.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1083+3114dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580213 | ||||||
| chr6:106580213
|
C | CAA | 53 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(50): Show | 56 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.1083+3113_1083+311 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580213 | ||||||
| chr6:106580213
|
C | CAAA | 6 | a0001c0003t0004g0170a0001c0003t0004g0178a0001c0003t0004g0179others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+3112_1083+311 others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580213 | ||||||
| chr6:106580213
|
CA | C | 9 | a0001c0001t0001g0278a0001c0001t0002g0078a0001c0002t0001g0188others(6): Show | 9 | HG00323.hp1 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+3114delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580213 | ||||||
| chr6:106580337
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0271 | 2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1083+2991T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580337 | ||||||
| chr6:106580424
|
A | C | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1083+2904T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580424 | ||||||
| chr6:106580467
|
C | G | 2 | a0001c0001t0002g0064a0001c0001t0002g0065 | 2 | HG02165.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1083+2861G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580467 | ||||||
| chr6:106580471
|
C | T | 209 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(206): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1083+2857G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580471 | ||||||
| chr6:106580501
|
C | T | 112 | a0001c0002t0001g0011a0001c0002t0005g0001a0001c0002t0005g0323others(109): Show | 120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1083+2827G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580501 | ||||||
| chr6:106580564
|
C | T | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1083+2764G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580564 | ||||||
| chr6:106580603
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1083+2725G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580603 | ||||||
| chr6:106580662
|
T | G | 1 | a0001c0004t0003g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1083+2666A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580662 | ||||||
| chr6:106580709
|
ACT | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1083+2617_1083+261 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580709 | ||||||
| chr6:106580711
|
T | A | 1 | a0001c0001t0002g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1083+2617A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580711 | ||||||
| chr6:106580718
|
C | CA | 35 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0325others(32): Show | 39 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1083+2609dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580718 | ||||||
| chr6:106580718
|
C | CAA | 3 | a0001c0002t0005g0328a0001c0002t0005g0343a0001c0002t0005g0345 | 3 | HG02074.hp1 NA18998.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1083+2608_1083+260 others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580718 | ||||||
| chr6:106580722
|
G | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1083+2606C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580722 | ||||||
| chr6:106580722
|
G | GA | 31 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0250others(28): Show | 32 | HG00438.hp2 HG00639.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1083+2605dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580722 | ||||||
| chr6:106580738
|
C | A | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.1083+2590G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580738 | ||||||
| chr6:106580750
|
T | A | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.1083+2578A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580750 | ||||||
| chr6:106580764
|
T | C | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.1083+2564A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580764 | ||||||
| chr6:106580964
|
T | G | 113 | a0001c0001t0001g0297a0001c0002t0001g0011a0001c0002t0005g0001others(110): Show | 121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1083+2364A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580964 | ||||||
| chr6:106580980
|
T | TA | 36 | a0001c0001t0001g0293a0001c0001t0001g0296a0001c0001t0006g0362others(33): Show | 38 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1083+2347dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580980 | ||||||
| chr6:106580980
|
TA | T | 76 | a0001c0001t0002g0048a0001c0001t0002g0063a0001c0002t0001g0011others(73): Show | 80 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(77): Show |
intron_variant | MODIFIER | c.1083+2347delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106580980 | ||||||
| chr6:106581116
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1083+2212A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581116 | ||||||
| chr6:106581277
|
T | A | 1 | a0001c0001t0008g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1083+2051A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581277 | ||||||
| chr6:106581283
|
G | A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+2045C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581283 | ||||||
| chr6:106581551
|
C | G | 1 | a0001c0005t0009g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1083+1777G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581551 | ||||||
| chr6:106581575
|
T | C | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1083+1753A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581575 | ||||||
| chr6:106581643
|
A | G | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1083+1685T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581643 | ||||||
| chr6:106581876
|
C | A | 1 | a0001c0005t0009g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1083+1452G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581876 | ||||||
| chr6:106581975
|
A | G | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1083+1353T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106581975 | ||||||
| chr6:106582229
|
G | A | 1 | a0001c0002t0005g0335 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1083+1099C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582229 | ||||||
| chr6:106582304
|
A | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1083+1024T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582304 | ||||||
| chr6:106582495
|
G | A | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1083+833C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582495 | ||||||
| chr6:106582587
|
T | TATAAGTC others(41): Show |
1 | a0001c0001t0002g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1083+693_1083+740d others(50): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582587 | ||||||
| chr6:106582592
|
G | C | 1 | a0001c0001t0001g0287 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1083+736C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582592 | ||||||
| chr6:106582688
|
C | G | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1083+640G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582688 | ||||||
| chr6:106582797
|
C | T | 112 | a0001c0002t0001g0011a0001c0002t0005g0001a0001c0002t0005g0323others(109): Show | 120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1083+531G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582797 | ||||||
| chr6:106582817
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1083+511G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106582817 | ||||||
| chr6:106583071
|
C | T | 1 | a0001c0003t0004g0172 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1083+257G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583071 | ||||||
| chr6:106583097
|
G | A | 4 | a0001c0002t0001g0191a0001c0002t0001g0194a0001c0002t0001g0198others(1): Show | 4 | HG01496.hp1 HG01928.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+231C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583097 | ||||||
| chr6:106583104
|
C | T | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1083+224G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583104 | ||||||
| chr6:106583124
|
T | C | 2 | a0001c0001t0008g0043a0001c0001t0008g0044 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1083+204A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583124 | ||||||
| chr6:106583179
|
G | C | 2 | a0001c0002t0010g0358a0001c0002t0010g0360 | 2 | HG01243.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1083+149C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583179 | ||||||
| chr6:106583251
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1083+77C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583251 | ||||||
| chr6:106583258
|
A | C | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1083+70T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 8/8 | chr6 | 106583258 | ||||||
| chr6:106583436
|
C | T | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.991-16G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583436 | ||||||
| chr6:106583449
|
A | G | 1 | a0001c0002t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.991-29T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583449 | ||||||
| chr6:106583621
|
A | C | 1 | a0001c0002t0001g0196 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.991-201T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583621 | ||||||
| chr6:106583785
|
T | G | 1 | a0001c0003t0004g0182 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.991-365A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583785 | ||||||
| chr6:106583891
|
C | T | 2 | a0001c0001t0002g0036a0001c0001t0002g0073 | 2 | HG00733.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.991-471G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583891 | ||||||
| chr6:106583994
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.991-574G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106583994 | ||||||
| chr6:106584007
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.991-587T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584007 | ||||||
| chr6:106584045
|
T | C | 1 | a0001c0002t0001g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.991-625A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584045 | ||||||
| chr6:106584078
|
C | A | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.991-658G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584078 | ||||||
| chr6:106584229
|
G | A | 2 | a0001c0001t0001g0285a0001c0001t0001g0291 | 2 | NA18993.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.991-809C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584229 | ||||||
| chr6:106584253
|
T | G | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-833A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584253 | ||||||
| chr6:106584485
|
G | A | 1 | a0001c0002t0005g0343 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.991-1065C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584485 | ||||||
| chr6:106584487
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.991-1067C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584487 | ||||||
| chr6:106584543
|
T | C | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-1123A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584543 | ||||||
| chr6:106584691
|
G | A | 320 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(317): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.991-1271C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106584691 | ||||||
| chr6:106585225
|
A | C | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.991-1805T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585225 | ||||||
| chr6:106585231
|
T | C | 1 | a0001c0003t0004g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.991-1811A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585231 | ||||||
| chr6:106585281
|
T | C | 112 | a0001c0002t0001g0011a0001c0002t0005g0001a0001c0002t0005g0323others(109): Show | 120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.991-1861A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585281 | ||||||
| chr6:106585291
|
C | T | 112 | a0001c0002t0001g0011a0001c0002t0005g0001a0001c0002t0005g0323others(109): Show | 120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.991-1871G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585291 | ||||||
| chr6:106585330
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.991-1910T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585330 | ||||||
| chr6:106585413
|
CAGA | C | 7 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0257others(4): Show | 7 | HG02258.hp1 HG02717.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-1996_991-1994d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585413 | ||||||
| chr6:106585443
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.991-2023C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585443 | ||||||
| chr6:106585542
|
A | C | 35 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(32): Show | 39 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.991-2122T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585542 | ||||||
| chr6:106585549
|
G | A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-2129C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585549 | ||||||
| chr6:106585594
|
A | T | 99 | a0001c0002t0001g0011a0001c0002t0005g0001a0001c0002t0005g0323others(96): Show | 107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.990+2085T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585594 | ||||||
| chr6:106585690
|
A | T | 1 | a0001c0003t0004g0158 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.990+1989T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585690 | ||||||
| chr6:106585695
|
G | A | 72 | a0001c0002t0001g0011a0001c0003t0004g0012a0001c0003t0004g0014others(69): Show | 76 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(73): Show |
intron_variant | MODIFIER | c.990+1984C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585695 | ||||||
| chr6:106585928
|
G | C | 1 | a0001c0002t0005g0352 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.990+1751C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106585928 | ||||||
| chr6:106586036
|
A | G | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.990+1643T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586036 | ||||||
| chr6:106586041
|
C | G | 34 | a0001c0001t0001g0269a0001c0004t0003g0002a0001c0004t0003g0003others(31): Show | 42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.990+1638G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586041 | ||||||
| chr6:106586051
|
C | T | 1 | a0001c0003t0004g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.990+1628G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586051 | ||||||
| chr6:106586088
|
A | G | 4 | a0001c0001t0002g0035a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 4 | NA18947.hp2 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+1591T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586088 | ||||||
| chr6:106586118
|
T | C | 21 | a0001c0001t0002g0020a0001c0001t0002g0045a0001c0001t0002g0048others(18): Show | 22 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.990+1561A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586118 | ||||||
| chr6:106586275
|
T | C | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.990+1404A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586275 | ||||||
| chr6:106586293
|
C | T | 3 | a0001c0002t0005g0345a0001c0003t0012g0349a0001c0003t0012g0356 | 3 | NA18942.hp1 NA18998.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.990+1386G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586293 | ||||||
| chr6:106586374
|
T | C | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.990+1305A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586374 | ||||||
| chr6:106586382
|
G | GT | 18 | a0001c0001t0001g0255a0001c0001t0001g0266a0001c0001t0002g0026others(15): Show | 18 | HG02135.hp2 HG02257.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.990+1296dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586382 | ||||||
| chr6:106586661
|
C | A | 1 | a0001c0001t0001g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.990+1018G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586661 | ||||||
| chr6:106586826
|
C | T | 29 | a0001c0003t0004g0014a0001c0003t0004g0015a0001c0003t0004g0142others(26): Show | 31 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.990+853G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586826 | ||||||
| chr6:106586913
|
T | G | 1 | a0001c0001t0001g0255 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.990+766A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586913 | ||||||
| chr6:106586914
|
G | T | 1 | a0001c0001t0001g0255 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.990+765C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106586914 | ||||||
| chr6:106587010
|
C | A | 208 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(205): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.990+669G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587010 | ||||||
| chr6:106587037
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.990+642G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587037 | ||||||
| chr6:106587111
|
G | A | 55 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(52): Show | 55 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.990+568C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587111 | ||||||
| chr6:106587135
|
C | T | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.990+544G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587135 | ||||||
| chr6:106587189
|
G | C | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.990+490C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587189 | ||||||
| chr6:106587319
|
G | T | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.990+360C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587319 | ||||||
| chr6:106587576
|
C | T | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.990+103G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 7/8 | chr6 | 106587576 | ||||||
| chr6:106587914
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0271 | 2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.807-52A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106587914 | ||||||
| chr6:106587991
|
G | A | 1 | a0001c0002t0001g0161 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.807-129C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106587991 | ||||||
| chr6:106588055
|
T | C | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-193A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588055 | ||||||
| chr6:106588197
|
CA | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-336delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588197 | ||||||
| chr6:106588353
|
A | G | 321 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(318): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.807-491T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588353 | ||||||
| chr6:106588456
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-594C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588456 | ||||||
| chr6:106588466
|
C | T | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0321 | 3 | HG02258.hp1 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.807-604G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588466 | ||||||
| chr6:106588516
|
C | CAAAAAAA others(340): Show |
1 | a0001c0004t0003g0129 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.807-655_807-654ins others(347): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588516 | ||||||
| chr6:106588686
|
G | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-824C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588686 | ||||||
| chr6:106588771
|
A | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-909T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588771 | ||||||
| chr6:106588782
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.807-920G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588782 | ||||||
| chr6:106588829
|
G | C | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.807-967C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588829 | ||||||
| chr6:106588881
|
C | T | 34 | a0001c0001t0001g0269a0001c0004t0003g0002a0001c0004t0003g0003others(31): Show | 42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.807-1019G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106588881 | ||||||
| chr6:106589006
|
A | G | 1 | a0001c0002t0001g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.807-1144T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589006 | ||||||
| chr6:106589034
|
C | T | 208 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(205): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.807-1172G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589034 | ||||||
| chr6:106589058
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.807-1196G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589058 | ||||||
| chr6:106589098
|
G | A | 2 | a0001c0003t0004g0217a0001c0003t0004g0221 | 2 | HG00639.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.807-1236C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589098 | ||||||
| chr6:106589102
|
C | T | 5 | a0001c0001t0001g0239a0001c0001t0001g0284a0001c0001t0001g0285others(2): Show | 5 | HG02135.hp1 NA18993.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.807-1240G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589102 | ||||||
| chr6:106589104
|
C | CAGAAGAA others(8): Show |
21 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0154others(18): Show | 22 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(19): Show |
intron_variant | MODIFIER | c.807-1257_807-1243d others(17): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589104 | ||||||
| chr6:106589104
|
CAGA | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1245_807-1243d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589104 | ||||||
| chr6:106589126
|
GGAA | G | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-1267_807-1265d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589126 | ||||||
| chr6:106589177
|
AGGAGGAG others(3): Show |
A | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.807-1325_807-1316d others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589177 | ||||||
| chr6:106589186
|
A | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1324T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589186 | ||||||
| chr6:106589187
|
G | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1325C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589187 | ||||||
| chr6:106589191
|
GGA | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1331_807-1330d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589191 | ||||||
| chr6:106589213
|
G | GGGA | 8 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0155others(5): Show | 9 | NA18950.hp2 NA18971.hp2 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-1354_807-1352d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589213 | ||||||
| chr6:106589219
|
A | G | 7 | a0001c0001t0002g0054a0001c0001t0002g0061a0001c0001t0002g0062others(4): Show | 7 | HG00639.hp1 HG00738.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.807-1357T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589219 | ||||||
| chr6:106589225
|
G | A | 271 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(268): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.807-1363C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589225 | ||||||
| chr6:106589226
|
A | G | 271 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(268): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.807-1364T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589226 | ||||||
| chr6:106589229
|
A | G | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.807-1367T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589229 | ||||||
| chr6:106589234
|
G | GAGGGAGG others(257): Show |
1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-1373_807-1372i others(266): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589234 | ||||||
| chr6:106589237
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-1375C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGACGAGG others(326): Show |
1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(335): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(406): Show |
1 | a0001c0001t0006g0372 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(415): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(365): Show |
1 | a0001c0001t0001g0255 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(374): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(349): Show |
2 | a0001c0001t0001g0235a0001c0001t0001g0259 | 2 | NA19009.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(358): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(329): Show |
1 | a0001c0001t0002g0058 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(338): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(366): Show |
1 | a0001c0001t0001g0267 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(375): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(330): Show |
1 | a0001c0001t0001g0283 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(339): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(356): Show |
17 | a0001c0001t0001g0016a0001c0001t0001g0238a0001c0001t0001g0245others(14): Show | 18 | HG00438.hp1 HG00597.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(365): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(368): Show |
1 | a0001c0001t0001g0306 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(377): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(312): Show |
2 | a0001c0001t0002g0008a0001c0001t0002g0040 | 3 | HG00280.hp1 HG01109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(321): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(354): Show |
1 | a0001c0001t0001g0234 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(363): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(369): Show |
46 | a0001c0001t0001g0005a0001c0001t0001g0232a0001c0001t0001g0236others(43): Show | 48 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(378): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(369): Show |
2 | a0001c0001t0001g0290a0001c0001t0001g0305 | 2 | NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(378): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(369): Show |
1 | a0001c0001t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(378): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(370): Show |
1 | a0001c0001t0001g0282 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(371): Show |
1 | a0001c0001t0001g0239 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(380): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(359): Show |
1 | a0001c0001t0001g0314 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(368): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(370): Show |
1 | a0001c0001t0001g0295 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(396): Show |
1 | a0001c0001t0001g0240 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(405): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(389): Show |
3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0299 | 3 | HG00408.hp2 NA18999.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(398): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(373): Show |
1 | a0001c0001t0001g0309 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(382): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(349): Show |
1 | a0001c0001t0001g0266 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(358): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(349): Show |
1 | a0001c0001t0001g0275 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(358): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(371): Show |
1 | a0001c0001t0001g0247 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(380): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(357): Show |
1 | a0001c0001t0001g0258 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(366): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(228): Show |
9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(237): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(231): Show |
1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(240): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(176): Show |
1 | a0001c0003t0004g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(185): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(191): Show |
20 | a0001c0003t0004g0154a0001c0003t0004g0158a0001c0003t0004g0167others(17): Show | 20 | HG01891.hp2 HG02074.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(200): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(206): Show |
2 | a0001c0003t0004g0180a0001c0003t0004g0181 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(215): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(167): Show |
2 | a0001c0003t0004g0223a0001c0003t0004g0226 | 2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(176): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(182): Show |
26 | a0001c0003t0004g0014a0001c0003t0004g0015a0001c0003t0004g0142others(23): Show | 28 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(191): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(377): Show |
1 | a0001c0002t0001g0163 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(386): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(212): Show |
1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(221): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(297): Show |
1 | a0001c0002t0005g0325 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(306): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(346): Show |
1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(355): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(359): Show |
1 | a0001c0002t0001g0201 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(368): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(338): Show |
1 | a0001c0002t0001g0193 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(347): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(330): Show |
2 | a0001c0001t0002g0072a0001c0001t0002g0085 | 2 | HG00735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(339): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(345): Show |
1 | a0001c0001t0002g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(354): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(350): Show |
1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(359): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(350): Show |
1 | a0001c0001t0001g0320 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(359): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(365): Show |
1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(374): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(375): Show |
3 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0200 | 3 | HG02451.hp1 HG02976.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(384): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(367): Show |
4 | a0001c0001t0002g0035a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 4 | NA18947.hp2 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(376): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(358): Show |
1 | a0001c0002t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(367): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(358): Show |
1 | a0001c0002t0001g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(367): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(343): Show |
1 | a0004c0007t0001g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(352): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(358): Show |
19 | a0001c0001t0001g0293a0001c0002t0001g0010a0001c0002t0001g0013others(16): Show | 21 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(367): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(358): Show |
2 | a0001c0004t0003g0096a0001c0004t0003g0097 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(367): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(365): Show |
1 | a0001c0001t0002g0051 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(374): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(371): Show |
1 | a0001c0002t0001g0192 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(380): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(350): Show |
35 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(32): Show | 35 | HG00140.hp2 HG00733.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(359): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(365): Show |
2 | a0001c0001t0002g0062a0001c0001t0002g0090 | 2 | HG00323.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(374): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(363): Show |
1 | a0001c0001t0002g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(372): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(370): Show |
1 | a0001c0001t0001g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(370): Show |
1 | a0001c0001t0002g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(370): Show |
1 | a0001c0001t0002g0033 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(379): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(398): Show |
1 | a0001c0002t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(407): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(380): Show |
1 | a0001c0001t0002g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(389): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(415): Show |
5 | a0001c0001t0006g0363a0001c0001t0006g0365a0001c0001t0006g0366others(2): Show | 5 | HG01099.hp2 HG02258.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(424): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(441): Show |
1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(450): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(425): Show |
3 | a0001c0001t0006g0362a0001c0001t0008g0019a0001c0001t0008g0042 | 3 | HG00544.hp1 HG01175.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(434): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(354): Show |
1 | a0001c0001t0002g0052 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(363): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(402): Show |
1 | a0001c0001t0002g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(411): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(331): Show |
1 | a0001c0001t0002g0071 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(340): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(405): Show |
1 | a0001c0001t0006g0371 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(414): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(350): Show |
5 | a0001c0001t0002g0028a0001c0001t0002g0031a0001c0001t0002g0032others(2): Show | 5 | HG02602.hp1 HG02698.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(359): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(405): Show |
1 | a0001c0001t0011g0006 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(414): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(405): Show |
1 | a0001c0001t0006g0364 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(414): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(410): Show |
2 | a0001c0001t0008g0043a0001c0001t0008g0044 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(419): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(416): Show |
1 | a0001c0001t0011g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(425): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(385): Show |
2 | a0001c0001t0006g0367a0001c0001t0006g0368 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(394): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(362): Show |
1 | a0001c0002t0001g0160 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(371): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(194): Show |
7 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0155others(4): Show | 8 | NA18950.hp2 NA18971.hp2 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(203): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(172): Show |
1 | a0001c0003t0004g0212 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(181): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(201): Show |
1 | a0001c0003t0004g0175 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(210): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(277): Show |
1 | a0001c0002t0005g0323 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(286): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(297): Show |
1 | a0001c0002t0005g0324 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(306): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(267): Show |
1 | a0001c0002t0005g0339 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(276): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(272): Show |
1 | a0001c0002t0005g0347 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(281): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(287): Show |
24 | a0001c0002t0005g0001a0001c0002t0005g0327a0001c0002t0005g0328others(21): Show | 28 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(296): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(275): Show |
1 | a0001c0002t0005g0335 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(284): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(288): Show |
1 | a0001c0002t0005g0326 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(288): Show |
1 | a0001c0002t0005g0336 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(288): Show |
1 | a0001c0002t0005g0340 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(288): Show |
1 | a0001c0002t0005g0344 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(307): Show |
1 | a0001c0002t0005g0352 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(316): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(336): Show |
1 | a0001c0001t0001g0318 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(345): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(288): Show |
1 | a0001c0002t0005g0337 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(297): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(346): Show |
2 | a0001c0001t0001g0319a0001c0001t0001g0321 | 2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(355): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(373): Show |
1 | a0001c0002t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(382): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGAGG others(415): Show |
1 | a0001c0001t0008g0089 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(424): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGAGGGAG others(372): Show |
1 | a0001c0002t0001g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.807-1376_807-1375i others(381): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGGAGGAG others(158): Show |
8 | a0001c0004t0003g0003a0001c0004t0003g0098a0001c0004t0003g0100others(5): Show | 10 | HG00609.hp2 HG02083.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(167): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGGAGGAG others(159): Show |
38 | a0001c0001t0001g0269a0001c0001t0002g0007a0001c0001t0002g0022others(35): Show | 45 | HG00423.hp2 HG00544.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.807-1376_807-1375i others(168): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGGAGGAG others(160): Show |
1 | a0001c0004t0003g0108 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(169): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGGAGGAG others(146): Show |
1 | a0001c0004t0003g0134 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(155): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGGAGGAG others(160): Show |
1 | a0001c0004t0003g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.807-1376_807-1375i others(169): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGGGGAGG others(382): Show |
2 | a0001c0002t0010g0359a0001c0002t0010g0361 | 2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(391): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589237
|
G | GGGGGAGG others(382): Show |
2 | a0001c0002t0010g0358a0001c0002t0010g0360 | 2 | HG01243.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.807-1376_807-1375i others(391): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589237 | ||||||
| chr6:106589238
|
G | GGAGGAGG others(221): Show |
1 | a0001c0004t0003g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.807-1377_807-1376i others(230): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589238 | ||||||
| chr6:106589242
|
G | A | 21 | a0001c0001t0002g0020a0001c0001t0002g0045a0001c0001t0002g0048others(18): Show | 22 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.807-1380C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589242 | ||||||
| chr6:106589251
|
A | AAGG | 42 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(39): Show | 46 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.807-1392_807-1390d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589251 | ||||||
| chr6:106589251
|
A | G | 1 | a0001c0004t0003g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.807-1389T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589251 | ||||||
| chr6:106589263
|
A | AAGAAGGA others(32): Show |
1 | a0001c0001t0001g0283 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.807-1402_807-1401i others(41): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589263 | ||||||
| chr6:106589266
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0002g0033 | 2 | HG01257.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.807-1404C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589266 | ||||||
| chr6:106589269
|
A | G | 2 | a0001c0003t0004g0223a0001c0003t0004g0226 | 2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.807-1407T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589269 | ||||||
| chr6:106589272
|
A | G | 2 | a0001c0003t0004g0223a0001c0003t0004g0226 | 2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.807-1410T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589272 | ||||||
| chr6:106589275
|
A | G | 2 | a0001c0001t0002g0033a0001c0002t0001g0011 | 3 | HG03453.hp1 NA18747.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.807-1413T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589275 | ||||||
| chr6:106589278
|
G | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0083a0001c0002t0001g0011 | 4 | HG03453.hp1 HG03704.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.807-1416C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589278 | ||||||
| chr6:106589278
|
G | GAGA | 270 | a0001c0001t0001g0016a0001c0001t0001g0232a0001c0001t0001g0234others(267): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.807-1419_807-1417d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589278 | ||||||
| chr6:106589278
|
G | GAGAAGAA others(8): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0254a0001c0001t0001g0255others(1): Show | 6 | NA18952.hp2 NA18978.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.807-1417_807-1416i others(17): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589278 | ||||||
| chr6:106589289
|
A | G | 42 | a0001c0001t0001g0291a0001c0002t0005g0001a0001c0002t0005g0323others(39): Show | 46 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.807-1427T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589289 | ||||||
| chr6:106589290
|
G | A | 41 | a0001c0001t0001g0291a0001c0002t0005g0001a0001c0002t0005g0323others(38): Show | 45 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.807-1428C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589290 | ||||||
| chr6:106589292
|
G | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1430C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589292 | ||||||
| chr6:106589293
|
A | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.807-1431T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589293 | ||||||
| chr6:106589303
|
G | A | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1441C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589303 | ||||||
| chr6:106589304
|
G | A | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1442C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589304 | ||||||
| chr6:106589305
|
A | G | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1443T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589305 | ||||||
| chr6:106589306
|
G | A | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1444C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589306 | ||||||
| chr6:106589309
|
G | A | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1447C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589309 | ||||||
| chr6:106589312
|
G | A | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1450C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589312 | ||||||
| chr6:106589315
|
G | A | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1453C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589315 | ||||||
| chr6:106589318
|
A | G | 2 | a0001c0001t0001g0291a0001c0003t0004g0223 | 2 | HG02055.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.807-1456T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589318 | ||||||
| chr6:106589321
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.807-1459C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589321 | ||||||
| chr6:106589324
|
A | G | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1462T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589324 | ||||||
| chr6:106589327
|
A | G | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-1465T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589327 | ||||||
| chr6:106589398
|
C | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-1536G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589398 | ||||||
| chr6:106589596
|
C | T | 1 | a0001c0002t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.807-1734G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589596 | ||||||
| chr6:106589712
|
C | T | 208 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(205): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.807-1850G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589712 | ||||||
| chr6:106589790
|
A | G | 1 | a0001c0002t0005g0345 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.807-1928T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589790 | ||||||
| chr6:106589834
|
C | T | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-1972G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589834 | ||||||
| chr6:106589938
|
C | T | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.807-2076G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589938 | ||||||
| chr6:106589968
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.807-2106T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106589968 | ||||||
| chr6:106590112
|
G | T | 1 | a0001c0004t0003g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.806+2052C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590112 | ||||||
| chr6:106590126
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.806+2038G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590126 | ||||||
| chr6:106590272
|
G | A | 2 | a0001c0002t0001g0231a0001c0003t0004g0179 | 2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.806+1892C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590272 | ||||||
| chr6:106590445
|
G | T | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.806+1719C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590445 | ||||||
| chr6:106590450
|
T | C | 259 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(256): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.806+1714A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590450 | ||||||
| chr6:106590468
|
G | A | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.806+1696C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590468 | ||||||
| chr6:106590531
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.806+1633T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590531 | ||||||
| chr6:106590579
|
G | C | 1 | a0001c0002t0001g0195 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.806+1585C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590579 | ||||||
| chr6:106590606
|
T | C | 1 | a0001c0001t0008g0089 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.806+1558A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590606 | ||||||
| chr6:106590652
|
T | A | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.806+1512A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590652 | ||||||
| chr6:106590693
|
C | T | 22 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0154others(19): Show | 23 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(20): Show |
intron_variant | MODIFIER | c.806+1471G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590693 | ||||||
| chr6:106590714
|
C | CA | 6 | a0001c0002t0005g0344a0001c0003t0004g0159a0001c0003t0004g0220others(3): Show | 6 | HG01884.hp1 NA18963.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+1449dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | ||||||
| chr6:106590714
|
C | CAA | 88 | a0001c0002t0001g0165a0001c0002t0001g0191a0001c0002t0005g0001others(85): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.806+1448_806+1449d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | ||||||
| chr6:106590714
|
C | CAAA | 40 | a0001c0001t0001g0256a0001c0001t0001g0289a0001c0001t0001g0293others(37): Show | 42 | HG00280.hp1 HG00438.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.806+1447_806+1449d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | ||||||
| chr6:106590714
|
C | CAAAA | 133 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(130): Show | 138 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.806+1446_806+1449d others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | ||||||
| chr6:106590714
|
C | CAAAAA | 24 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0267others(21): Show | 24 | HG00140.hp1 HG01074.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.806+1445_806+1449d others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | ||||||
| chr6:106590714
|
C | CAAAAAA | 29 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0032others(26): Show | 30 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.806+1444_806+1449d others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590714 | ||||||
| chr6:106590783
|
G | C | 219 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(216): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.806+1381C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590783 | ||||||
| chr6:106590796
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.806+1368C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590796 | ||||||
| chr6:106590809
|
C | G | 1 | a0001c0003t0004g0175 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.806+1355G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590809 | ||||||
| chr6:106590839
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.806+1325C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590839 | ||||||
| chr6:106590846
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.806+1318G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590846 | ||||||
| chr6:106590847
|
G | A | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.806+1317C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590847 | ||||||
| chr6:106590908
|
G | A | 1 | a0001c0003t0004g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.806+1256C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590908 | ||||||
| chr6:106590993
|
A | T | 1 | a0001c0004t0003g0127 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.806+1171T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106590993 | ||||||
| chr6:106591051
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0310 | 2 | NA18998.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.806+1113G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591051 | ||||||
| chr6:106591210
|
C | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(86): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.806+954G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591210 | ||||||
| chr6:106591349
|
C | T | 5 | a0001c0003t0004g0168a0001c0003t0004g0207a0001c0003t0004g0208others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.806+815G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591349 | ||||||
| chr6:106591393
|
G | C | 1 | a0001c0004t0003g0116 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.806+771C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591393 | ||||||
| chr6:106591420
|
C | CTT | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.806+742_806+743dup others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591420 | ||||||
| chr6:106591429
|
C | T | 1 | a0001c0003t0004g0175 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.806+735G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591429 | ||||||
| chr6:106591430
|
T | C | 1 | a0001c0003t0004g0175 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.806+734A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591430 | ||||||
| chr6:106591443
|
T | G | 1 | a0001c0001t0001g0281 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.806+721A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591443 | ||||||
| chr6:106591553
|
C | T | 55 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(52): Show | 55 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.806+611G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591553 | ||||||
| chr6:106591575
|
A | T | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.806+589T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591575 | ||||||
| chr6:106591580
|
G | C | 1 | a0001c0001t0001g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.806+584C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591580 | ||||||
| chr6:106591652
|
C | T | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.806+512G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591652 | ||||||
| chr6:106591699
|
T | A | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.806+465A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591699 | ||||||
| chr6:106591699
|
T | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.806+465A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591699 | ||||||
| chr6:106591845
|
G | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.806+319C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 6/8 | chr6 | 106591845 | ||||||
| chr6:106592304
|
C | T | 1 | a0001c0002t0001g0197 | 1 | HG02523.hp2 | splice_region_variant&intron_variant | LOW | c.670-4G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592304 | ||||||
| chr6:106592386
|
T | C | 1 | a0001c0002t0001g0196 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.670-86A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592386 | ||||||
| chr6:106592415
|
G | A | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.670-115C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592415 | ||||||
| chr6:106592428
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.670-128C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592428 | ||||||
| chr6:106592588
|
G | A | 1 | a0001c0003t0004g0143 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.670-288C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592588 | ||||||
| chr6:106592645
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0320 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.670-345G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592645 | ||||||
| chr6:106592657
|
C | T | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.670-357G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592657 | ||||||
| chr6:106592690
|
G | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-390C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592690 | ||||||
| chr6:106592929
|
C | CA | 41 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(38): Show | 45 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.670-630dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592929 | ||||||
| chr6:106592936
|
A | C | 1 | a0001c0001t0002g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.670-636T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106592936 | ||||||
| chr6:106593093
|
C | T | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-793G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593093 | ||||||
| chr6:106593099
|
G | C | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.670-799C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593099 | ||||||
| chr6:106593100
|
C | T | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.670-800G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593100 | ||||||
| chr6:106593201
|
T | C | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.670-901A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593201 | ||||||
| chr6:106593327
|
A | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.670-1027T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593327 | ||||||
| chr6:106593418
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670-1118C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593418 | ||||||
| chr6:106593493
|
A | C | 2 | a0001c0003t0004g0214a0001c0003t0004g0218 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.670-1193T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593493 | ||||||
| chr6:106593547
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1247A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593547 | ||||||
| chr6:106593552
|
A | C | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1252T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593552 | ||||||
| chr6:106593556
|
G | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1256C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593556 | ||||||
| chr6:106593558
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1258A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593558 | ||||||
| chr6:106593559
|
A | T | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1259T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593559 | ||||||
| chr6:106593568
|
C | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1268G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593568 | ||||||
| chr6:106593570
|
C | T | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1270G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593570 | ||||||
| chr6:106593573
|
G | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1273C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593573 | ||||||
| chr6:106593576
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1276A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593576 | ||||||
| chr6:106593578
|
C | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1278G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593578 | ||||||
| chr6:106593580
|
AGGGATCT others(52): Show |
A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1339_670-1281d others(61): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593580 | ||||||
| chr6:106593642
|
G | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1342C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593642 | ||||||
| chr6:106593643
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1343A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593643 | ||||||
| chr6:106593647
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1347A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593647 | ||||||
| chr6:106593648
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1348A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593648 | ||||||
| chr6:106593649
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1349A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593649 | ||||||
| chr6:106593650
|
C | T | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1350G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593650 | ||||||
| chr6:106593651
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1351A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593651 | ||||||
| chr6:106593652
|
G | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1352C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593652 | ||||||
| chr6:106593653
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1353A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593653 | ||||||
| chr6:106593654
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1354A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593654 | ||||||
| chr6:106593660
|
C | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1360G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593660 | ||||||
| chr6:106593665
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1365A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593665 | ||||||
| chr6:106593667
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1367A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593667 | ||||||
| chr6:106593671
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1371A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593671 | ||||||
| chr6:106593672
|
A | G | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1372T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593672 | ||||||
| chr6:106593676
|
G | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1376C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593676 | ||||||
| chr6:106593677
|
G | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1377C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593677 | ||||||
| chr6:106593678
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1378A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593678 | ||||||
| chr6:106593679
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1379A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593679 | ||||||
| chr6:106593680
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1380A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593680 | ||||||
| chr6:106593681
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1381A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593681 | ||||||
| chr6:106593682
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1382A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593682 | ||||||
| chr6:106593689
|
T | TAAAAAAA others(59): Show |
1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1390_670-1389i others(68): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593689 | ||||||
| chr6:106593693
|
T | A | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1393A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593693 | ||||||
| chr6:106593694
|
A | T | 1 | a0001c0003t0007g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670-1394T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593694 | ||||||
| chr6:106593779
|
A | C | 1 | a0001c0001t0002g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.670-1479T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593779 | ||||||
| chr6:106593846
|
G | A | 2 | a0001c0002t0001g0186a0001c0002t0001g0187 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.670-1546C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593846 | ||||||
| chr6:106593880
|
A | C | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-1580T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106593880 | ||||||
| chr6:106594068
|
T | C | 1 | a0001c0004t0003g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.670-1768A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594068 | ||||||
| chr6:106594081
|
G | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.670-1781C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594081 | ||||||
| chr6:106594229
|
G | A | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.670-1929C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594229 | ||||||
| chr6:106594326
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.670-2026T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594326 | ||||||
| chr6:106594384
|
C | T | 1 | a0005c0010t0013g0018 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.670-2084G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594384 | ||||||
| chr6:106594438
|
G | A | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-2138C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594438 | ||||||
| chr6:106594491
|
C | G | 1 | a0001c0004t0003g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.670-2191G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594491 | ||||||
| chr6:106594527
|
A | G | 2 | a0001c0001t0001g0318a0001c0001t0001g0321 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.670-2227T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594527 | ||||||
| chr6:106594527
|
AAAAG | A | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-2231_670-2228d others(6): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594527 | ||||||
| chr6:106594537
|
A | C | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.670-2237T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594537 | ||||||
| chr6:106594579
|
C | A | 311 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(308): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.670-2279G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594579 | ||||||
| chr6:106594691
|
T | A | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-2391A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594691 | ||||||
| chr6:106594794
|
T | C | 1 | a0001c0004t0003g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.670-2494A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594794 | ||||||
| chr6:106594846
|
G | A | 1 | a0001c0001t0008g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.670-2546C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594846 | ||||||
| chr6:106594988
|
T | G | 320 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(317): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.670-2688A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106594988 | ||||||
| chr6:106595052
|
T | G | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-2752A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595052 | ||||||
| chr6:106595055
|
G | A | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.670-2755C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595055 | ||||||
| chr6:106595065
|
A | G | 259 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(256): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.670-2765T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595065 | ||||||
| chr6:106595116
|
A | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.670-2816T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595116 | ||||||
| chr6:106595134
|
T | C | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG02523.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.670-2834A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595134 | ||||||
| chr6:106595150
|
T | G | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-2850A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595150 | ||||||
| chr6:106595194
|
T | G | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-2894A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595194 | ||||||
| chr6:106595287
|
C | A | 20 | a0001c0002t0005g0323a0001c0002t0005g0326a0001c0002t0005g0327others(17): Show | 20 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.670-2987G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595287 | ||||||
| chr6:106595327
|
A | T | 1 | a0001c0001t0002g0046 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.670-3027T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595327 | ||||||
| chr6:106595408
|
A | G | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.670-3108T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595408 | ||||||
| chr6:106595419
|
C | G | 1 | a0001c0001t0001g0314 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.670-3119G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595419 | ||||||
| chr6:106595496
|
CTTTCT | C | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-3201_670-3197d others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595496 | ||||||
| chr6:106595500
|
C | CT | 6 | a0001c0003t0004g0154a0001c0003t0004g0178a0001c0003t0004g0211others(3): Show | 6 | HG00544.hp2 HG02559.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-3201dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595500 | ||||||
| chr6:106595500
|
CT | C | 205 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(202): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.670-3201delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595500 | ||||||
| chr6:106595500
|
CTT | C | 37 | a0001c0001t0001g0255a0001c0002t0005g0001a0001c0002t0005g0323others(34): Show | 41 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.670-3202_670-3201d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595500 | ||||||
| chr6:106595521
|
G | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-3221C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595521 | ||||||
| chr6:106595558
|
C | T | 207 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(204): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.670-3258G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595558 | ||||||
| chr6:106595623
|
G | A | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.670-3323C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595623 | ||||||
| chr6:106595631
|
GAGATTAC others(1): Show |
G | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-3339_670-3332d others(10): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595631 | ||||||
| chr6:106595632
|
A | G | 254 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(251): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.670-3332T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595632 | ||||||
| chr6:106595642
|
T | A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-3342A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595642 | ||||||
| chr6:106595686
|
A | C | 258 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(255): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.670-3386T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595686 | ||||||
| chr6:106595823
|
C | T | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-3523G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595823 | ||||||
| chr6:106595872
|
A | C | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-3572T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595872 | ||||||
| chr6:106595876
|
A | C | 258 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(255): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.670-3576T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595876 | ||||||
| chr6:106595894
|
C | G | 1 | a0001c0002t0005g0330 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.670-3594G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106595894 | ||||||
| chr6:106596038
|
CATT | C | 207 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(204): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.670-3741_670-3739d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596038 | ||||||
| chr6:106596061
|
C | T | 321 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(318): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.670-3761G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596061 | ||||||
| chr6:106596206
|
TAAG | T | 207 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(204): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.670-3909_670-3907d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596206 | ||||||
| chr6:106596318
|
A | G | 1 | a0001c0003t0004g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.670-4018T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596318 | ||||||
| chr6:106596366
|
T | C | 2 | a0001c0002t0001g0186a0001c0002t0001g0187 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.670-4066A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596366 | ||||||
| chr6:106596400
|
C | G | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.670-4100G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596400 | ||||||
| chr6:106596426
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.670-4126C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596426 | ||||||
| chr6:106596429
|
A | G | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.670-4129T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596429 | ||||||
| chr6:106596667
|
A | C | 61 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(58): Show | 64 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.670-4367T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596667 | ||||||
| chr6:106596798
|
C | A | 1 | a0001c0001t0001g0286 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.670-4498G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596798 | ||||||
| chr6:106596957
|
T | A | 1 | a0001c0001t0001g0240 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670-4657A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596957 | ||||||
| chr6:106596981
|
C | T | 11 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(8): Show | 11 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.670-4681G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106596981 | ||||||
| chr6:106597135
|
T | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-4835A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597135 | ||||||
| chr6:106597217
|
T | C | 2 | a0001c0004t0003g0134a0001c0004t0003g0136 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.670-4917A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597217 | ||||||
| chr6:106597298
|
A | C | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-4998T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597298 | ||||||
| chr6:106597301
|
T | C | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.670-5001A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597301 | ||||||
| chr6:106597339
|
C | A | 364 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(361): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.670-5039G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597339 | ||||||
| chr6:106597564
|
G | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670-5264C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597564 | ||||||
| chr6:106597565
|
AATCGCTG others(1729): Show |
A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3573_670-5266d others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597565 | ||||||
| chr6:106597625
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+5249C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597625 | ||||||
| chr6:106597691
|
C | CT | 8 | a0001c0001t0001g0238a0001c0001t0001g0258a0001c0001t0001g0261others(5): Show | 8 | HG02572.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+5182dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597691 | ||||||
| chr6:106597691
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.669+5183G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597691 | ||||||
| chr6:106597702
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0286 | 2 | NA18986.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.669+5172A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597702 | ||||||
| chr6:106597740
|
A | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+5134T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597740 | ||||||
| chr6:106597784
|
C | T | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.669+5090G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597784 | ||||||
| chr6:106597829
|
A | G | 1 | a0001c0004t0003g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.669+5045T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597829 | ||||||
| chr6:106597830
|
C | T | 102 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(99): Show | 109 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.669+5044G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597830 | ||||||
| chr6:106597854
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+5020G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597854 | ||||||
| chr6:106597993
|
A | G | 89 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(86): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.669+4881T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106597993 | ||||||
| chr6:106598017
|
G | A | 1 | a0001c0002t0001g0191 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.669+4857C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598017 | ||||||
| chr6:106598020
|
T | C | 1 | a0001c0002t0001g0191 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.669+4854A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598020 | ||||||
| chr6:106598050
|
A | G | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.669+4824T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598050 | ||||||
| chr6:106598072
|
A | C | 1 | a0001c0001t0001g0253 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.669+4802T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598072 | ||||||
| chr6:106598132
|
T | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+4742A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598132 | ||||||
| chr6:106598145
|
G | A | 5 | a0001c0001t0002g0086a0001c0005t0009g0094a0001c0005t0009g0095others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+4729C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598145 | ||||||
| chr6:106598166
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.669+4708C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598166 | ||||||
| chr6:106598309
|
C | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+4565G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598309 | ||||||
| chr6:106598351
|
G | A | 1 | a0001c0003t0004g0182 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.669+4523C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598351 | ||||||
| chr6:106598413
|
T | C | 1 | a0001c0005t0009g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.669+4461A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598413 | ||||||
| chr6:106598447
|
T | C | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.669+4427A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598447 | ||||||
| chr6:106598454
|
G | T | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+4420C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598454 | ||||||
| chr6:106598620
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0307 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.669+4254G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598620 | ||||||
| chr6:106598651
|
G | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(86): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.669+4223C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598651 | ||||||
| chr6:106598836
|
C | T | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+4038G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598836 | ||||||
| chr6:106598941
|
C | T | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+3933G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106598941 | ||||||
| chr6:106599027
|
ATTTAT | A | 5 | a0001c0003t0004g0015a0001c0003t0004g0224a0001c0003t0004g0225others(2): Show | 6 | HG01891.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+3842_669+3846d others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599027 | ||||||
| chr6:106599317
|
A | G | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3557T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599317 | ||||||
| chr6:106599319
|
C | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3555G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599319 | ||||||
| chr6:106599323
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3551A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599323 | ||||||
| chr6:106599325
|
T | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3549A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599325 | ||||||
| chr6:106599326
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3548A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599326 | ||||||
| chr6:106599331
|
T | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3543A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599331 | ||||||
| chr6:106599338
|
T | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3536A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599338 | ||||||
| chr6:106599341
|
T | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3533A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599341 | ||||||
| chr6:106599342
|
C | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3532G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599342 | ||||||
| chr6:106599347
|
T | G | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3527A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599347 | ||||||
| chr6:106599352
|
A | G | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3522T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599352 | ||||||
| chr6:106599354
|
T | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3520A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599354 | ||||||
| chr6:106599355
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3519A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599355 | ||||||
| chr6:106599356
|
A | T | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3518T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599356 | ||||||
| chr6:106599358
|
A | T | 184 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(181): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.669+3516T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599358 | ||||||
| chr6:106599360
|
T | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3514A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599360 | ||||||
| chr6:106599362
|
C | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+3512G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599362 | ||||||
| chr6:106599365
|
CCTGTGTC others(1930): Show |
C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1572_669+3508d others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599365 | ||||||
| chr6:106599448
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.669+3426A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599448 | ||||||
| chr6:106599451
|
C | CT | 211 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(208): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.669+3422dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599451 | ||||||
| chr6:106599460
|
T | C | 4 | a0001c0005t0009g0094a0001c0005t0009g0095a0001c0005t0009g0131others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+3414A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599460 | ||||||
| chr6:106599502
|
C | T | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+3372G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599502 | ||||||
| chr6:106599545
|
G | C | 256 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(253): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.669+3329C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599545 | ||||||
| chr6:106599561
|
T | TTGCATCT others(339): Show |
1 | a0001c0001t0002g0033 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.669+3312_669+3313i others(348): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599561 | ||||||
| chr6:106599596
|
G | A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+3278C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599596 | ||||||
| chr6:106599680
|
T | A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+3194A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599680 | ||||||
| chr6:106599684
|
C | T | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+3190G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599684 | ||||||
| chr6:106599710
|
T | C | 1 | a0001c0002t0001g0010 | 2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.669+3164A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599710 | ||||||
| chr6:106599772
|
T | C | 216 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(213): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.669+3102A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599772 | ||||||
| chr6:106599773
|
G | A | 3 | a0001c0001t0002g0054a0001c0001t0002g0063a0001c0001t0002g0070 | 3 | HG01934.hp2 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.669+3101C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599773 | ||||||
| chr6:106599835
|
C | T | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+3039G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599835 | ||||||
| chr6:106599835
|
CCTT | C | 38 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(35): Show | 42 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.669+3036_669+3038d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599835 | ||||||
| chr6:106599836
|
C | CT | 11 | a0001c0001t0001g0240a0001c0001t0001g0256a0001c0003t0007g0144others(8): Show | 11 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+3037dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599836 | ||||||
| chr6:106599836
|
C | T | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+3038G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599836 | ||||||
| chr6:106599836
|
CT | C | 6 | a0001c0001t0001g0238a0001c0001t0001g0242a0001c0001t0001g0286others(3): Show | 6 | HG02523.hp2 HG02572.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+3037delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599836 | ||||||
| chr6:106599998
|
G | A | 21 | a0001c0001t0002g0020a0001c0001t0002g0045a0001c0001t0002g0048others(18): Show | 22 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.669+2876C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106599998 | ||||||
| chr6:106600014
|
T | A | 1 | a0001c0002t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.669+2860A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600014 | ||||||
| chr6:106600067
|
A | G | 59 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(56): Show | 62 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.669+2807T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600067 | ||||||
| chr6:106600088
|
C | G | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+2786G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600088 | ||||||
| chr6:106600090
|
C | T | 4 | a0001c0001t0002g0035a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 4 | NA18947.hp2 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+2784G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600090 | ||||||
| chr6:106600095
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.669+2779G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600095 | ||||||
| chr6:106600148
|
T | C | 1 | a0001c0005t0009g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+2726A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600148 | ||||||
| chr6:106600167
|
G | C | 216 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(213): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.669+2707C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600167 | ||||||
| chr6:106600168
|
G | A | 5 | a0001c0001t0001g0239a0001c0001t0001g0284a0001c0001t0001g0285others(2): Show | 5 | HG02135.hp1 NA18993.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+2706C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600168 | ||||||
| chr6:106600285
|
G | C | 13 | a0001c0003t0004g0014a0001c0003t0004g0142a0001c0003t0004g0166others(10): Show | 14 | HG02135.hp2 HG02148.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.669+2589C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600285 | ||||||
| chr6:106600286
|
T | G | 316 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(313): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.669+2588A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600286 | ||||||
| chr6:106600609
|
T | G | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.669+2265A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600609 | ||||||
| chr6:106600618
|
TTC | T | 5 | a0001c0001t0001g0244a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | HG02056.hp2 HG02083.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+2254_669+2255d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600618 | ||||||
| chr6:106600681
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.669+2193C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600681 | ||||||
| chr6:106600737
|
G | A | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.669+2137C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600737 | ||||||
| chr6:106600774
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.669+2100A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600774 | ||||||
| chr6:106600834
|
C | A | 1 | a0001c0001t0001g0264 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.669+2040G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600834 | ||||||
| chr6:106600840
|
C | T | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+2034G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600840 | ||||||
| chr6:106600883
|
G | T | 1 | a0001c0001t0001g0273 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.669+1991C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600883 | ||||||
| chr6:106600918
|
A | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+1956T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600918 | ||||||
| chr6:106600937
|
G | T | 1 | a0001c0001t0001g0273 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.669+1937C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600937 | ||||||
| chr6:106600968
|
C | T | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.669+1906G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106600968 | ||||||
| chr6:106601008
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.669+1866T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601008 | ||||||
| chr6:106601049
|
C | T | 7 | a0001c0003t0004g0015a0001c0003t0004g0224a0001c0003t0004g0225others(4): Show | 8 | HG01891.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.669+1825G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601049 | ||||||
| chr6:106601222
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.669+1652C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601222 | ||||||
| chr6:106601307
|
G | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1567C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601307 | ||||||
| chr6:106601308
|
G | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1566C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601308 | ||||||
| chr6:106601310
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1564A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601310 | ||||||
| chr6:106601312
|
C | G | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1562G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601312 | ||||||
| chr6:106601313
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1561A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601313 | ||||||
| chr6:106601318
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1556A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601318 | ||||||
| chr6:106601319
|
C | T | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1555G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601319 | ||||||
| chr6:106601331
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1543A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601331 | ||||||
| chr6:106601332
|
G | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1542C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601332 | ||||||
| chr6:106601334
|
T | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1540A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601334 | ||||||
| chr6:106601338
|
G | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1536C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601338 | ||||||
| chr6:106601342
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1532A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601342 | ||||||
| chr6:106601345
|
T | G | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1529A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601345 | ||||||
| chr6:106601346
|
T | C | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1528A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601346 | ||||||
| chr6:106601349
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1525A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601349 | ||||||
| chr6:106601352
|
C | T | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1522G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601352 | ||||||
| chr6:106601356
|
C | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1518G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601356 | ||||||
| chr6:106601358
|
G | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1516C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601358 | ||||||
| chr6:106601361
|
G | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1513C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601361 | ||||||
| chr6:106601362
|
G | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1512C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601362 | ||||||
| chr6:106601363
|
T | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+1511A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601363 | ||||||
| chr6:106601401
|
A | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+1473T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601401 | ||||||
| chr6:106601468
|
A | C | 1 | a0001c0002t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669+1406T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601468 | ||||||
| chr6:106601491
|
T | A | 23 | a0001c0001t0002g0020a0001c0001t0002g0045a0001c0001t0002g0048others(20): Show | 25 | HG00544.hp1 HG00642.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.669+1383A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601491 | ||||||
| chr6:106601641
|
G | T | 319 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(316): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.669+1233C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601641 | ||||||
| chr6:106601672
|
G | A | 63 | a0001c0001t0002g0020a0001c0001t0002g0045a0001c0001t0002g0048others(60): Show | 69 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.669+1202C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601672 | ||||||
| chr6:106601684
|
T | C | 319 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(316): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.669+1190A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601684 | ||||||
| chr6:106601692
|
C | G | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+1182G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601692 | ||||||
| chr6:106601739
|
T | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+1135A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601739 | ||||||
| chr6:106601783
|
G | GT | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+1090dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601783 | ||||||
| chr6:106601814
|
T | A | 2 | a0001c0004t0003g0123a0001c0004t0003g0126 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.669+1060A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106601814 | ||||||
| chr6:106602061
|
T | C | 2 | a0001c0001t0002g0024a0001c0002t0001g0231 | 2 | HG02257.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.669+813A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602061 | ||||||
| chr6:106602076
|
T | G | 1 | a0001c0005t0009g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+798A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602076 | ||||||
| chr6:106602277
|
C | CA | 5 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(2): Show | 5 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+596dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602277 | ||||||
| chr6:106602288
|
C | G | 1 | a0001c0002t0001g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.669+586G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602288 | ||||||
| chr6:106602309
|
T | C | 1 | a0001c0002t0005g0324 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.669+565A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602309 | ||||||
| chr6:106602315
|
G | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+559C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602315 | ||||||
| chr6:106602600
|
C | T | 1 | a0001c0003t0004g0214 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.669+274G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602600 | ||||||
| chr6:106602621
|
A | G | 1 | a0001c0003t0004g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.669+253T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602621 | ||||||
| chr6:106602826
|
T | G | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+48A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602826 | ||||||
| chr6:106602857
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.669+17A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 5/8 | chr6 | 106602857 | ||||||
| chr6:106602982
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0307 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.621-60C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106602982 | ||||||
| chr6:106602992
|
A | T | 319 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(316): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.621-70T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106602992 | ||||||
| chr6:106603071
|
G | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0055a0001c0001t0002g0056 | 3 | HG02109.hp2 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.621-149C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603071 | ||||||
| chr6:106603135
|
T | C | 1 | a0001c0001t0006g0365 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.621-213A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603135 | ||||||
| chr6:106603148
|
T | A | 1 | a0001c0001t0002g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.621-226A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603148 | ||||||
| chr6:106603156
|
C | T | 3 | a0001c0001t0001g0238a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG02572.hp2 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.621-234G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603156 | ||||||
| chr6:106603265
|
G | C | 1 | a0001c0002t0001g0202 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.621-343C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603265 | ||||||
| chr6:106603344
|
C | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(202): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.621-422G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603344 | ||||||
| chr6:106603482
|
C | T | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.621-560G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603482 | ||||||
| chr6:106603572
|
G | A | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621-650C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603572 | ||||||
| chr6:106603621
|
C | A | 1 | a0001c0001t0001g0306 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.621-699G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603621 | ||||||
| chr6:106603632
|
A | G | 1 | a0001c0001t0002g0080 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.621-710T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603632 | ||||||
| chr6:106603680
|
T | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-758A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603680 | ||||||
| chr6:106603710
|
T | C | 1 | a0001c0002t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.621-788A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603710 | ||||||
| chr6:106603897
|
G | T | 1 | a0001c0001t0002g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.621-975C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106603897 | ||||||
| chr6:106604091
|
C | A | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.621-1169G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604091 | ||||||
| chr6:106604185
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.621-1263G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604185 | ||||||
| chr6:106604198
|
A | G | 7 | a0001c0003t0004g0015a0001c0003t0004g0224a0001c0003t0004g0225others(4): Show | 8 | HG01891.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.621-1276T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604198 | ||||||
| chr6:106604209
|
C | T | 2 | a0001c0001t0002g0064a0001c0001t0002g0065 | 2 | HG02165.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.621-1287G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604209 | ||||||
| chr6:106604224
|
A | G | 1 | a0001c0003t0004g0219 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.621-1302T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604224 | ||||||
| chr6:106604351
|
C | T | 1 | a0001c0003t0004g0167 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.621-1429G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604351 | ||||||
| chr6:106604404
|
C | A | 1 | a0001c0001t0001g0301 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.621-1482G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604404 | ||||||
| chr6:106604427
|
T | G | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.621-1505A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604427 | ||||||
| chr6:106604450
|
A | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(202): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.621-1528T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604450 | ||||||
| chr6:106604454
|
A | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.621-1532T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604454 | ||||||
| chr6:106604505
|
C | T | 1 | a0001c0003t0007g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.621-1583G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604505 | ||||||
| chr6:106604579
|
T | C | 1 | a0001c0002t0005g0355 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.621-1657A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604579 | ||||||
| chr6:106604630
|
A | G | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.621-1708T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604630 | ||||||
| chr6:106604665
|
A | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-1743T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604665 | ||||||
| chr6:106604677
|
T | G | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-1755A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604677 | ||||||
| chr6:106604686
|
T | A | 1 | a0001c0004t0003g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.621-1764A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604686 | ||||||
| chr6:106604760
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.621-1838T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604760 | ||||||
| chr6:106604851
|
T | C | 1 | a0001c0002t0005g0329 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.621-1929A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106604851 | ||||||
| chr6:106605161
|
C | T | 3 | a0001c0003t0004g0207a0001c0003t0004g0208a0001c0003t0004g0210 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.621-2239G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605161 | ||||||
| chr6:106605424
|
C | CA | 45 | a0001c0001t0001g0235a0001c0001t0001g0246a0001c0001t0001g0259others(42): Show | 49 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.621-2503dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605424 | ||||||
| chr6:106605446
|
A | G | 6 | a0001c0001t0002g0054a0001c0001t0002g0061a0001c0001t0002g0062others(3): Show | 6 | HG00639.hp1 HG00738.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-2524T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605446 | ||||||
| chr6:106605496
|
T | C | 2 | a0001c0003t0004g0214a0001c0003t0004g0218 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.621-2574A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605496 | ||||||
| chr6:106605571
|
T | C | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621-2649A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605571 | ||||||
| chr6:106605609
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.621-2687G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605609 | ||||||
| chr6:106605671
|
G | T | 2 | a0001c0001t0011g0006a0001c0001t0011g0021 | 3 | HG02109.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.621-2749C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605671 | ||||||
| chr6:106605731
|
A | G | 256 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(253): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.621-2809T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605731 | ||||||
| chr6:106605741
|
C | T | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.621-2819G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605741 | ||||||
| chr6:106605752
|
G | A | 1 | a0001c0003t0004g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.621-2830C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605752 | ||||||
| chr6:106605773
|
C | T | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-2851G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605773 | ||||||
| chr6:106605813
|
T | TCA | 16 | a0001c0003t0004g0156a0001c0003t0004g0158a0001c0003t0004g0167others(13): Show | 16 | HG01106.hp2 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.621-2892_621-2891i others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605813 | ||||||
| chr6:106605814
|
C | CA | 23 | a0001c0001t0002g0022a0001c0002t0005g0001a0001c0002t0005g0325others(20): Show | 27 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.621-2893_621-2892i others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | ||||||
| chr6:106605814
|
CCCAAAA | C | 8 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(5): Show | 9 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.621-2898_621-2893d others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | ||||||
| chr6:106605814
|
CCCAAAAA | C | 37 | a0001c0001t0001g0269a0001c0004t0003g0002a0001c0004t0003g0003others(34): Show | 44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.621-2899_621-2893d others(9): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | ||||||
| chr6:106605814
|
CCCAAAAA others(2): Show |
C | 4 | a0001c0001t0002g0024a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 4 | HG00140.hp2 HG02738.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.621-2901_621-2893d others(11): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | ||||||
| chr6:106605814
|
CCCAAAAA others(3): Show |
C | 55 | a0001c0001t0001g0245a0001c0001t0001g0258a0001c0001t0001g0260others(52): Show | 55 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.621-2902_621-2893d others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | ||||||
| chr6:106605814
|
CCCAAAAA others(4): Show |
C | 156 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(153): Show | 164 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.621-2903_621-2893d others(13): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | ||||||
| chr6:106605814
|
CCCAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0308 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.621-2904_621-2893d others(14): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605814 | ||||||
| chr6:106605815
|
C | A | 84 | a0001c0001t0002g0007a0001c0001t0002g0041a0001c0002t0005g0323others(81): Show | 88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.621-2893G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605815 | ||||||
| chr6:106605816
|
C | A | 24 | a0001c0001t0002g0022a0001c0002t0005g0001a0001c0002t0005g0325others(21): Show | 28 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.621-2894G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605816 | ||||||
| chr6:106605816
|
C | CAA | 13 | a0001c0002t0005g0323a0001c0002t0005g0324a0001c0002t0005g0328others(10): Show | 13 | HG00408.hp1 HG00423.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.621-2896_621-2895d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605816 | ||||||
| chr6:106605817
|
A | AC | 42 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(39): Show | 45 | HG00280.hp2 HG00639.hp2 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.621-2896_621-2895i others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605817 | ||||||
| chr6:106605818
|
A | C | 3 | a0001c0003t0004g0177a0001c0003t0014g0017a0003c0012t0002g0091 | 3 | HG03209.hp2 NA18747.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.621-2896T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605818 | ||||||
| chr6:106605822
|
A | C | 8 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(5): Show | 9 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.621-2900T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605822 | ||||||
| chr6:106605823
|
A | C | 37 | a0001c0001t0001g0269a0001c0004t0003g0002a0001c0004t0003g0003others(34): Show | 44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.621-2901T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605823 | ||||||
| chr6:106605825
|
A | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 4 | HG00140.hp2 HG02738.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.621-2903T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605825 | ||||||
| chr6:106605826
|
A | C | 55 | a0001c0001t0001g0245a0001c0001t0001g0258a0001c0001t0001g0260others(52): Show | 55 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.621-2904T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605826 | ||||||
| chr6:106605827
|
A | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(153): Show | 164 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.621-2905T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605827 | ||||||
| chr6:106605828
|
A | C | 1 | a0001c0001t0001g0308 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.621-2906T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605828 | ||||||
| chr6:106605884
|
A | T | 1 | a0001c0001t0001g0272 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.621-2962T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605884 | ||||||
| chr6:106605895
|
G | A | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621-2973C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605895 | ||||||
| chr6:106605972
|
A | G | 7 | a0001c0003t0004g0015a0001c0003t0004g0224a0001c0003t0004g0225others(4): Show | 8 | HG01891.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.621-3050T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605972 | ||||||
| chr6:106605973
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.621-3051C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106605973 | ||||||
| chr6:106606122
|
C | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(202): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.621-3200G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606122 | ||||||
| chr6:106606228
|
C | T | 1 | a0001c0011t0004g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.621-3306G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606228 | ||||||
| chr6:106606263
|
A | G | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.621-3341T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606263 | ||||||
| chr6:106606292
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | NA18948.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.621-3370C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606292 | ||||||
| chr6:106606351
|
C | T | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.621-3429G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606351 | ||||||
| chr6:106606366
|
G | C | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.621-3444C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606366 | ||||||
| chr6:106606444
|
C | T | 255 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(252): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.621-3522G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606444 | ||||||
| chr6:106606635
|
G | A | 2 | a0001c0002t0005g0351a0001c0003t0004g0221 | 2 | HG01192.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.621-3713C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606635 | ||||||
| chr6:106606867
|
A | C | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.621-3945T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606867 | ||||||
| chr6:106606915
|
T | G | 1 | a0001c0003t0004g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621-3993A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606915 | ||||||
| chr6:106606961
|
T | C | 84 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(81): Show | 88 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.621-4039A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606961 | ||||||
| chr6:106606972
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621-4050C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606972 | ||||||
| chr6:106606996
|
A | T | 216 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(213): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.621-4074T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106606996 | ||||||
| chr6:106607035
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.621-4113T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607035 | ||||||
| chr6:106607036
|
C | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0245a0001c0001t0001g0258others(8): Show | 12 | HG00438.hp1 HG02071.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.621-4114G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607036 | ||||||
| chr6:106607283
|
C | CA | 42 | a0001c0001t0002g0034a0001c0001t0002g0078a0001c0002t0005g0001others(39): Show | 46 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.621-4362dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607283 | ||||||
| chr6:106607486
|
T | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.621-4564A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607486 | ||||||
| chr6:106607529
|
CA | C | 256 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(253): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.621-4608delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607529 | ||||||
| chr6:106607565
|
G | T | 1 | a0001c0003t0004g0212 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.621-4643C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607565 | ||||||
| chr6:106607707
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.621-4785G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607707 | ||||||
| chr6:106607721
|
T | C | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.621-4799A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607721 | ||||||
| chr6:106607815
|
T | C | 20 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0154others(17): Show | 21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.621-4893A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607815 | ||||||
| chr6:106607826
|
CA | C | 61 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(58): Show | 64 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.621-4905delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607826 | ||||||
| chr6:106607832
|
A | T | 1 | a0001c0001t0001g0293 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.621-4910T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607832 | ||||||
| chr6:106607833
|
A | G | 61 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(58): Show | 64 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.621-4911T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607833 | ||||||
| chr6:106607865
|
G | T | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.621-4943C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607865 | ||||||
| chr6:106607952
|
G | A | 319 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(316): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.621-5030C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106607952 | ||||||
| chr6:106608031
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621-5109G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608031 | ||||||
| chr6:106608285
|
A | C | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.621-5363T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608285 | ||||||
| chr6:106608494
|
T | C | 9 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(6): Show | 9 | HG02451.hp1 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-5572A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608494 | ||||||
| chr6:106608526
|
T | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(273): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.621-5604A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608526 | ||||||
| chr6:106608622
|
C | T | 1 | a0001c0003t0007g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.621-5700G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608622 | ||||||
| chr6:106608651
|
T | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-5729A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608651 | ||||||
| chr6:106608783
|
G | GA | 8 | a0001c0004t0003g0002a0001c0004t0003g0105a0001c0004t0003g0115others(5): Show | 11 | HG01192.hp1 HG01255.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.621-5862dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106608783 | ||||||
| chr6:106609097
|
C | T | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-6175G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609097 | ||||||
| chr6:106609161
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621-6239A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609161 | ||||||
| chr6:106609305
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.621-6383C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609305 | ||||||
| chr6:106609392
|
G | A | 41 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(38): Show | 45 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.621-6470C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609392 | ||||||
| chr6:106609599
|
G | A | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.621-6677C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609599 | ||||||
| chr6:106609651
|
A | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0271 | 2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.621-6729T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609651 | ||||||
| chr6:106609680
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.621-6758A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609680 | ||||||
| chr6:106609716
|
C | A | 1 | a0001c0001t0001g0269 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.621-6794G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609716 | ||||||
| chr6:106609869
|
C | A | 1 | a0001c0003t0004g0182 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.621-6947G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609869 | ||||||
| chr6:106609900
|
A | AC | 6 | a0001c0003t0004g0173a0001c0003t0004g0214a0001c0003t0004g0216others(3): Show | 6 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-6979dupG | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609900 | ||||||
| chr6:106609906
|
A | T | 1 | a0001c0002t0005g0332 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.621-6984T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609906 | ||||||
| chr6:106609973
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0265 | 2 | HG00558.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.621-7051T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609973 | ||||||
| chr6:106609980
|
G | A | 1 | a0001c0005t0009g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.621-7058C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106609980 | ||||||
| chr6:106610067
|
AT | A | 65 | a0001c0001t0002g0053a0001c0002t0010g0358a0001c0002t0010g0359others(62): Show | 68 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.621-7146delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610067 | ||||||
| chr6:106610101
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.621-7179C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610101 | ||||||
| chr6:106610342
|
G | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-7420C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610342 | ||||||
| chr6:106610362
|
C | T | 217 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(214): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.621-7440G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610362 | ||||||
| chr6:106610394
|
C | A | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.621-7472G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610394 | ||||||
| chr6:106610517
|
A | C | 55 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(52): Show | 55 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.621-7595T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610517 | ||||||
| chr6:106610529
|
G | C | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621-7607C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610529 | ||||||
| chr6:106610621
|
G | A | 38 | a0001c0002t0001g0163a0001c0002t0001g0199a0001c0002t0005g0001others(35): Show | 42 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.621-7699C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610621 | ||||||
| chr6:106610689
|
T | TCAAAATC others(314): Show |
2 | a0001c0004t0003g0135a0001c0004t0003g0136 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.621-7768_621-7767i others(323): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610689 | ||||||
| chr6:106610689
|
T | TCAAAATC others(315): Show |
2 | a0001c0004t0003g0133a0001c0004t0003g0134 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.621-7768_621-7767i others(324): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610689 | ||||||
| chr6:106610702
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621-7780C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610702 | ||||||
| chr6:106610746
|
G | C | 1 | a0001c0001t0006g0372 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.621-7824C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610746 | ||||||
| chr6:106610954
|
T | G | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621-8032A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610954 | ||||||
| chr6:106610994
|
G | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.621-8072C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106610994 | ||||||
| chr6:106611035
|
C | G | 205 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(202): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.621-8113G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611035 | ||||||
| chr6:106611048
|
C | CA | 42 | a0001c0001t0001g0263a0001c0001t0001g0305a0001c0001t0006g0365others(39): Show | 47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.621-8127dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611048 | ||||||
| chr6:106611060
|
C | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.621-8138G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611060 | ||||||
| chr6:106611168
|
G | A | 1 | a0001c0003t0007g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.620+8034C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611168 | ||||||
| chr6:106611178
|
G | A | 1 | a0001c0004t0003g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.620+8024C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611178 | ||||||
| chr6:106611278
|
T | C | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+7924A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611278 | ||||||
| chr6:106611346
|
T | C | 3 | a0001c0004t0003g0127a0001c0004t0003g0128a0001c0004t0003g0129 | 3 | HG01192.hp1 HG01255.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.620+7856A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611346 | ||||||
| chr6:106611387
|
G | A | 1 | a0001c0003t0004g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.620+7815C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611387 | ||||||
| chr6:106611582
|
T | C | 41 | a0001c0001t0001g0259a0001c0002t0005g0001a0001c0002t0005g0323others(38): Show | 45 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.620+7620A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611582 | ||||||
| chr6:106611596
|
C | G | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+7606G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611596 | ||||||
| chr6:106611596
|
C | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(81): Show | 88 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.620+7606G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611596 | ||||||
| chr6:106611735
|
C | T | 1 | a0001c0004t0003g0127 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.620+7467G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611735 | ||||||
| chr6:106611779
|
T | A | 1 | a0001c0002t0001g0183 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.620+7423A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106611779 | ||||||
| chr6:106612008
|
G | C | 60 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(57): Show | 63 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.620+7194C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612008 | ||||||
| chr6:106612016
|
C | A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+7186G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612016 | ||||||
| chr6:106612088
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.620+7114C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612088 | ||||||
| chr6:106612112
|
C | T | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+7090G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612112 | ||||||
| chr6:106612184
|
C | T | 1 | a0004c0007t0001g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.620+7018G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612184 | ||||||
| chr6:106612211
|
A | AC | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+6990dupG | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612211 | ||||||
| chr6:106612272
|
A | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+6930T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612272 | ||||||
| chr6:106612279
|
C | T | 1 | a0001c0003t0004g0171 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.620+6923G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612279 | ||||||
| chr6:106612384
|
C | CA | 70 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0236others(67): Show | 71 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.620+6817dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | ||||||
| chr6:106612384
|
C | CAA | 7 | a0001c0001t0001g0270a0001c0001t0001g0320a0001c0001t0002g0020others(4): Show | 7 | HG01517.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+6816_620+6817d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | ||||||
| chr6:106612384
|
CA | C | 53 | a0001c0001t0001g0253a0001c0001t0001g0267a0001c0001t0001g0269others(50): Show | 62 | HG00544.hp2 HG00597.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.620+6817delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | ||||||
| chr6:106612384
|
CAA | C | 21 | a0001c0002t0001g0011a0001c0003t0004g0012a0001c0003t0004g0154others(18): Show | 23 | HG00280.hp2 HG02074.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.620+6816_620+6817d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | ||||||
| chr6:106612384
|
CAAAAAAA others(10): Show |
C | 4 | a0001c0004t0003g0133a0001c0004t0003g0134a0001c0004t0003g0135others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+6801_620+6817d others(19): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612384 | ||||||
| chr6:106612480
|
G | A | 1 | a0001c0003t0004g0173 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.620+6722C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612480 | ||||||
| chr6:106612559
|
C | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(86): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.620+6643G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612559 | ||||||
| chr6:106612560
|
G | A | 1 | a0001c0004t0003g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.620+6642C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612560 | ||||||
| chr6:106612563
|
T | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0244a0001c0001t0001g0245others(15): Show | 19 | HG00438.hp1 HG02056.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.620+6639A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612563 | ||||||
| chr6:106612655
|
T | TACCTACT others(21): Show |
319 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(316): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.620+6546_620+6547i others(30): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612655 | ||||||
| chr6:106612855
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+6347C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612855 | ||||||
| chr6:106612864
|
G | A | 205 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(202): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.620+6338C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612864 | ||||||
| chr6:106612892
|
A | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0052 | 2 | NA18991.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.620+6310T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612892 | ||||||
| chr6:106612933
|
T | A | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+6269A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612933 | ||||||
| chr6:106612961
|
T | C | 216 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(213): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.620+6241A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106612961 | ||||||
| chr6:106613013
|
C | T | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+6189G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613013 | ||||||
| chr6:106613257
|
C | T | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+5945G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613257 | ||||||
| chr6:106613341
|
T | C | 371 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(368): Show | 395 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.620+5861A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613341 | ||||||
| chr6:106613387
|
G | A | 6 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0120others(3): Show | 9 | HG02056.hp1 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.620+5815C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613387 | ||||||
| chr6:106613455
|
C | T | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+5747G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613455 | ||||||
| chr6:106613569
|
A | C | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+5633T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613569 | ||||||
| chr6:106613677
|
T | G | 1 | a0001c0003t0007g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.620+5525A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613677 | ||||||
| chr6:106613756
|
A | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+5446T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613756 | ||||||
| chr6:106613783
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.620+5419C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106613783 | ||||||
| chr6:106614081
|
G | C | 1 | a0001c0001t0001g0253 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.620+5121C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614081 | ||||||
| chr6:106614312
|
T | C | 40 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(37): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.620+4890A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614312 | ||||||
| chr6:106614357
|
T | C | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+4845A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614357 | ||||||
| chr6:106614454
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.620+4748A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614454 | ||||||
| chr6:106614482
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.620+4720C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614482 | ||||||
| chr6:106614487
|
A | C | 1 | a0001c0001t0006g0365 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.620+4715T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614487 | ||||||
| chr6:106614543
|
C | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0307 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.620+4659G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614543 | ||||||
| chr6:106614600
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.620+4602G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614600 | ||||||
| chr6:106614609
|
G | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(202): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.620+4593C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614609 | ||||||
| chr6:106614853
|
T | C | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | NA18948.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.620+4349A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614853 | ||||||
| chr6:106614883
|
C | T | 1 | a0001c0004t0003g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.620+4319G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614883 | ||||||
| chr6:106614952
|
A | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(273): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.620+4250T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614952 | ||||||
| chr6:106614952
|
A | T | 1 | a0001c0001t0001g0312 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.620+4250T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614952 | ||||||
| chr6:106614959
|
A | AC | 13 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.620+4242dupG | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614959 | ||||||
| chr6:106614959
|
A | C | 1 | a0001c0011t0004g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.620+4243T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614959 | ||||||
| chr6:106614965
|
C | G | 2 | a0001c0003t0004g0169a0001c0003t0004g0211 | 2 | NA18966.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.620+4237G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106614965 | ||||||
| chr6:106615006
|
G | C | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+4196C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615006 | ||||||
| chr6:106615014
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.620+4188A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615014 | ||||||
| chr6:106615127
|
C | A | 8 | a0001c0003t0004g0015a0001c0003t0004g0224a0001c0003t0004g0225others(5): Show | 9 | HG01891.hp1 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.620+4075G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615127 | ||||||
| chr6:106615216
|
G | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+3986C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615216 | ||||||
| chr6:106615287
|
C | T | 191 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0257others(188): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.620+3915G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615287 | ||||||
| chr6:106615344
|
A | G | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.620+3858T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615344 | ||||||
| chr6:106615408
|
C | CA | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+3793dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615408 | ||||||
| chr6:106615544
|
A | G | 222 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(219): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.620+3658T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615544 | ||||||
| chr6:106615568
|
G | A | 2 | a0001c0002t0001g0163a0001c0008t0001g0153 | 2 | HG01516.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.620+3634C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615568 | ||||||
| chr6:106615665
|
A | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(209): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.620+3537T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615665 | ||||||
| chr6:106615683
|
G | A | 211 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(208): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.620+3519C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615683 | ||||||
| chr6:106615783
|
C | T | 211 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(208): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.620+3419G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615783 | ||||||
| chr6:106615784
|
G | A | 211 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(208): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.620+3418C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615784 | ||||||
| chr6:106615856
|
C | T | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+3346G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615856 | ||||||
| chr6:106615886
|
T | C | 30 | a0001c0003t0004g0014a0001c0003t0004g0015a0001c0003t0004g0142others(27): Show | 32 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.620+3316A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106615886 | ||||||
| chr6:106616006
|
A | G | 1 | a0001c0004t0003g0102 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.620+3196T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616006 | ||||||
| chr6:106616007
|
C | T | 33 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(30): Show | 41 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.620+3195G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616007 | ||||||
| chr6:106616025
|
C | T | 176 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(173): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.620+3177G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616025 | ||||||
| chr6:106616046
|
G | A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+3156C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616046 | ||||||
| chr6:106616076
|
G | A | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+3126C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616076 | ||||||
| chr6:106616277
|
A | C | 1 | a0001c0003t0004g0143 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.620+2925T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616277 | ||||||
| chr6:106616345
|
G | C | 1 | a0001c0001t0002g0040 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.620+2857C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616345 | ||||||
| chr6:106616360
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.620+2842A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616360 | ||||||
| chr6:106616566
|
CAATAGCT | C | 127 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(124): Show | 136 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.620+2629_620+2635d others(9): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616566 | ||||||
| chr6:106616576
|
T | C | 126 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(123): Show | 135 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.620+2626A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616576 | ||||||
| chr6:106616713
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.620+2489A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616713 | ||||||
| chr6:106616790
|
G | A | 2 | a0001c0008t0001g0153a0003c0012t0002g0091 | 2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.620+2412C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616790 | ||||||
| chr6:106616936
|
C | A | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+2266G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616936 | ||||||
| chr6:106616970
|
G | A | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+2232C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616970 | ||||||
| chr6:106616981
|
G | A | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+2221C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106616981 | ||||||
| chr6:106617013
|
A | AAG | 23 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(20): Show | 25 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.620+2187_620+2188d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617013 | ||||||
| chr6:106617054
|
T | C | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.620+2148A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617054 | ||||||
| chr6:106617202
|
T | A | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+2000A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617202 | ||||||
| chr6:106617225
|
A | G | 54 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(51): Show | 62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.620+1977T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617225 | ||||||
| chr6:106617239
|
A | C | 1 | a0001c0001t0001g0264 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.620+1963T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617239 | ||||||
| chr6:106617252
|
C | T | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+1950G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617252 | ||||||
| chr6:106617331
|
G | C | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+1871C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617331 | ||||||
| chr6:106617404
|
C | T | 54 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(51): Show | 62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.620+1798G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617404 | ||||||
| chr6:106617405
|
A | T | 1 | a0001c0001t0006g0365 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.620+1797T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617405 | ||||||
| chr6:106617411
|
T | C | 2 | a0001c0003t0004g0177a0001c0011t0004g0233 | 2 | NA18747.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.620+1791A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617411 | ||||||
| chr6:106617463
|
C | A | 2 | a0001c0008t0001g0153a0003c0012t0002g0091 | 2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.620+1739G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617463 | ||||||
| chr6:106617501
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.620+1701G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617501 | ||||||
| chr6:106617604
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+1598C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617604 | ||||||
| chr6:106617638
|
G | A | 54 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(51): Show | 62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.620+1564C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617638 | ||||||
| chr6:106617738
|
C | T | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+1464G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617738 | ||||||
| chr6:106617758
|
C | A | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+1444G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617758 | ||||||
| chr6:106617947
|
A | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620+1255T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106617947 | ||||||
| chr6:106618111
|
A | G | 1 | a0001c0002t0005g0330 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.620+1091T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618111 | ||||||
| chr6:106618115
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.620+1087G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618115 | ||||||
| chr6:106618127
|
T | A | 56 | a0001c0002t0001g0011a0001c0003t0014g0017a0001c0004t0003g0002others(53): Show | 65 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.620+1075A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618127 | ||||||
| chr6:106618133
|
T | C | 98 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(95): Show | 103 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.620+1069A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618133 | ||||||
| chr6:106618137
|
A | G | 98 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(95): Show | 103 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.620+1065T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618137 | ||||||
| chr6:106618227
|
CA | C | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+974delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618227 | ||||||
| chr6:106618282
|
T | TA | 55 | a0001c0002t0001g0011a0001c0004t0003g0002a0001c0004t0003g0003others(52): Show | 64 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.620+919dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618282 | ||||||
| chr6:106618282
|
TA | T | 87 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(84): Show | 90 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.620+919delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618282 | ||||||
| chr6:106618295
|
GTTATT | G | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+902_620+906del others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618295 | ||||||
| chr6:106618443
|
C | T | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+759G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618443 | ||||||
| chr6:106618580
|
A | G | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+622T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618580 | ||||||
| chr6:106618594
|
G | A | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.620+608C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618594 | ||||||
| chr6:106618618
|
A | C | 134 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(131): Show | 143 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.620+584T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618618 | ||||||
| chr6:106618624
|
G | A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+578C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618624 | ||||||
| chr6:106618668
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0320 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.620+534C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618668 | ||||||
| chr6:106618668
|
G | T | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+534C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618668 | ||||||
| chr6:106618678
|
T | C | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+524A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618678 | ||||||
| chr6:106618797
|
G | A | 4 | a0001c0003t0004g0178a0001c0003t0004g0179a0001c0003t0004g0180others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+405C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618797 | ||||||
| chr6:106618863
|
C | CT | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+338dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618863 | ||||||
| chr6:106618893
|
T | C | 3 | a0001c0004t0003g0127a0001c0004t0003g0128a0001c0004t0003g0129 | 3 | HG01192.hp1 HG01255.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.620+309A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106618893 | ||||||
| chr6:106619006
|
G | A | 52 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(49): Show | 60 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.620+196C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106619006 | ||||||
| chr6:106619023
|
T | C | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.620+179A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106619023 | ||||||
| chr6:106619098
|
C | T | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.620+104G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106619098 | ||||||
| chr6:106619124
|
C | A | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.620+78G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 4/8 | chr6 | 106619124 | ||||||
| chr6:106619544
|
CACA | C | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.496-221_496-219del others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619544 | ||||||
| chr6:106619570
|
T | A | 89 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(86): Show | 94 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.496-244A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619570 | ||||||
| chr6:106619589
|
T | TA | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-264dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619589 | ||||||
| chr6:106619595
|
T | A | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-269A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619595 | ||||||
| chr6:106619606
|
A | AT | 43 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(40): Show | 45 | HG00280.hp2 HG00597.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.496-281dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619606 | ||||||
| chr6:106619606
|
AT | A | 48 | a0001c0001t0001g0246a0001c0001t0001g0256a0001c0001t0001g0307others(45): Show | 50 | HG00438.hp2 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.496-281delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619606 | ||||||
| chr6:106619606
|
ATT | A | 36 | a0001c0002t0001g0163a0001c0002t0005g0001a0001c0002t0005g0323others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.496-282_496-281del others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619606 | ||||||
| chr6:106619606
|
ATTTT | A | 50 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(47): Show | 58 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.496-284_496-281del others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619606 | ||||||
| chr6:106619634
|
C | T | 1 | a0001c0003t0004g0156 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.496-308G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619634 | ||||||
| chr6:106619635
|
G | A | 1 | a0003c0012t0002g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.496-309C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619635 | ||||||
| chr6:106619684
|
T | C | 2 | a0001c0001t0002g0084a0001c0001t0002g0088 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.496-358A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619684 | ||||||
| chr6:106619701
|
T | C | 1 | a0001c0004t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.496-375A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619701 | ||||||
| chr6:106619705
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.496-379C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619705 | ||||||
| chr6:106619776
|
T | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.496-450A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619776 | ||||||
| chr6:106619778
|
AT | A | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-453delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619778 | ||||||
| chr6:106619813
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.496-487C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619813 | ||||||
| chr6:106619847
|
G | A | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-521C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619847 | ||||||
| chr6:106619857
|
C | T | 134 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(131): Show | 143 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.496-531G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619857 | ||||||
| chr6:106619890
|
C | T | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-564G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619890 | ||||||
| chr6:106619921
|
TTAA | T | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-598_496-596del others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619921 | ||||||
| chr6:106619951
|
G | T | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-625C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619951 | ||||||
| chr6:106619976
|
T | G | 1 | a0001c0004t0003g0130 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.496-650A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106619976 | ||||||
| chr6:106620070
|
T | A | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-744A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620070 | ||||||
| chr6:106620255
|
A | C | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-929T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620255 | ||||||
| chr6:106620357
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496-1031G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620357 | ||||||
| chr6:106620518
|
C | T | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.495+907G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620518 | ||||||
| chr6:106620558
|
C | T | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.495+867G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620558 | ||||||
| chr6:106620716
|
A | G | 2 | a0001c0001t0006g0362a0001c0001t0006g0363 | 2 | HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.495+709T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620716 | ||||||
| chr6:106620776
|
A | G | 1 | a0001c0003t0007g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.495+649T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620776 | ||||||
| chr6:106620826
|
G | A | 8 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(5): Show | 8 | HG01099.hp1 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+599C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620826 | ||||||
| chr6:106620904
|
C | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0055a0001c0001t0002g0056 | 3 | HG02109.hp2 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.495+521G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106620904 | ||||||
| chr6:106621071
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.495+354C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621071 | ||||||
| chr6:106621182
|
CA | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(83): Show | 89 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.495+242delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621182 | ||||||
| chr6:106621234
|
C | G | 20 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0154others(17): Show | 21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.495+191G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621234 | ||||||
| chr6:106621265
|
A | G | 3 | a0001c0005t0009g0094a0001c0005t0009g0095a0001c0005t0009g0131 | 3 | HG02615.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.495+160T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621265 | ||||||
| chr6:106621357
|
G | A | 368 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(365): Show | 391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.495+68C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621357 | ||||||
| chr6:106621383
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.495+42C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621383 | ||||||
| chr6:106621398
|
T | C | 190 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0013others(187): Show | 208 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.495+27A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 3/8 | chr6 | 106621398 | ||||||
| chr6:106621535
|
T | C | 20 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0154others(17): Show | 21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.427-42A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621535 | ||||||
| chr6:106621547
|
G | A | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.427-54C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621547 | ||||||
| chr6:106621576
|
T | G | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-83A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621576 | ||||||
| chr6:106621744
|
A | G | 2 | a0001c0004t0003g0096a0001c0004t0003g0097 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.427-251T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621744 | ||||||
| chr6:106621843
|
C | T | 1 | a0001c0002t0001g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.427-350G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106621843 | ||||||
| chr6:106622017
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.427-524A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622017 | ||||||
| chr6:106622074
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.427-581A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622074 | ||||||
| chr6:106622104
|
AAC | A | 20 | a0001c0003t0004g0014a0001c0003t0004g0142a0001c0003t0004g0166others(17): Show | 21 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.427-613_427-612del others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622104 | ||||||
| chr6:106622168
|
CA | C | 52 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(49): Show | 60 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.426+649delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622168 | ||||||
| chr6:106622286
|
T | C | 2 | a0001c0003t0014g0017a0003c0012t0002g0091 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.426+532A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622286 | ||||||
| chr6:106622354
|
T | A | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.426+464A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622354 | ||||||
| chr6:106622576
|
G | A | 52 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(49): Show | 60 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.426+242C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622576 | ||||||
| chr6:106622639
|
G | T | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.426+179C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622639 | ||||||
| chr6:106622653
|
C | T | 52 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(49): Show | 60 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.426+165G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622653 | ||||||
| chr6:106622745
|
C | T | 2 | a0001c0001t0002g0054a0001c0008t0001g0153 | 2 | HG01934.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.426+73G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622745 | ||||||
| chr6:106622790
|
G | A | 2 | a0001c0001t0002g0087a0001c0002t0001g0011 | 3 | HG00738.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.426+28C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 2/8 | chr6 | 106622790 | ||||||
| chr6:106623051
|
A | G | 36 | a0001c0002t0005g0001a0001c0002t0005g0323a0001c0002t0005g0324others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.275-82T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623051 | ||||||
| chr6:106623093
|
C | A | 21 | a0001c0003t0004g0014a0001c0003t0004g0142a0001c0003t0004g0166others(18): Show | 22 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.275-124G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623093 | ||||||
| chr6:106623149
|
ACT | A | 23 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(20): Show | 25 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.275-182_275-181del others(2): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623149 | ||||||
| chr6:106623239
|
G | A | 2 | a0001c0001t0011g0006a0001c0001t0011g0021 | 3 | HG02109.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.275-270C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623239 | ||||||
| chr6:106623309
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.275-340T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623309 | ||||||
| chr6:106623326
|
G | A | 1 | a0001c0002t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.275-357C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623326 | ||||||
| chr6:106623424
|
T | C | 1 | a0001c0003t0004g0143 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.275-455A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623424 | ||||||
| chr6:106623434
|
G | A | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.275-465C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623434 | ||||||
| chr6:106623472
|
G | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-503C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623472 | ||||||
| chr6:106623545
|
A | T | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-576T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623545 | ||||||
| chr6:106623601
|
T | A | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.275-632A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623601 | ||||||
| chr6:106623616
|
T | C | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.275-647A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623616 | ||||||
| chr6:106623720
|
T | A | 1 | a0001c0003t0004g0167 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.275-751A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623720 | ||||||
| chr6:106623760
|
T | C | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-791A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623760 | ||||||
| chr6:106623767
|
G | A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-798C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623767 | ||||||
| chr6:106623798
|
C | T | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-829G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623798 | ||||||
| chr6:106623799
|
A | G | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-830T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623799 | ||||||
| chr6:106623872
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.275-903A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623872 | ||||||
| chr6:106623901
|
G | C | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.275-932C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623901 | ||||||
| chr6:106623920
|
C | A | 194 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0013others(191): Show | 212 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.275-951G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623920 | ||||||
| chr6:106623967
|
T | C | 2 | a0001c0003t0004g0180a0001c0003t0004g0181 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.275-998A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106623967 | ||||||
| chr6:106624003
|
G | T | 1 | a0001c0002t0001g0183 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.275-1034C>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624003 | ||||||
| chr6:106624061
|
T | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-1092A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624061 | ||||||
| chr6:106624211
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.275-1242T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624211 | ||||||
| chr6:106624244
|
T | C | 194 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0013others(191): Show | 212 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.275-1275A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624244 | ||||||
| chr6:106624245
|
G | C | 53 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(50): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.275-1276C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624245 | ||||||
| chr6:106624259
|
T | A | 1 | a0005c0010t0013g0018 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.275-1290A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624259 | ||||||
| chr6:106624284
|
T | G | 194 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0013others(191): Show | 212 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.275-1315A>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624284 | ||||||
| chr6:106624289
|
C | T | 1 | a0001c0003t0004g0182 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.275-1320G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624289 | ||||||
| chr6:106624297
|
G | A | 1 | a0001c0003t0004g0182 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.275-1328C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624297 | ||||||
| chr6:106624300
|
C | T | 20 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0154others(17): Show | 21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.275-1331G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624300 | ||||||
| chr6:106624349
|
C | T | 20 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0154others(17): Show | 21 | HG02074.hp2 HG02559.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.275-1380G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624349 | ||||||
| chr6:106624398
|
C | T | 1 | a0001c0002t0005g0324 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.275-1429G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624398 | ||||||
| chr6:106624401
|
A | G | 347 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(344): Show | 369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.275-1432T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624401 | ||||||
| chr6:106624499
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-1530C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624499 | ||||||
| chr6:106624538
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.275-1569A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624538 | ||||||
| chr6:106624575
|
G | A | 2 | a0001c0003t0014g0017a0003c0012t0002g0091 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.275-1606C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624575 | ||||||
| chr6:106624616
|
G | A | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-1647C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624616 | ||||||
| chr6:106624746
|
A | C | 1 | a0001c0004t0003g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.275-1777T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624746 | ||||||
| chr6:106624756
|
T | C | 1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.275-1787A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624756 | ||||||
| chr6:106624839
|
G | A | 1 | a0001c0005t0009g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.275-1870C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624839 | ||||||
| chr6:106624898
|
T | A | 1 | a0005c0010t0013g0018 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.275-1929A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624898 | ||||||
| chr6:106624935
|
C | CA | 16 | a0001c0001t0001g0250a0001c0001t0001g0260a0001c0001t0001g0321others(13): Show | 17 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.275-1967dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624935 | ||||||
| chr6:106624936
|
A | G | 1 | a0001c0002t0010g0361 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.275-1967T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624936 | ||||||
| chr6:106624942
|
AAAAAAAA others(3): Show |
A | 4 | a0001c0002t0010g0358a0001c0002t0010g0359a0001c0002t0010g0360others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-1983_275-1974d others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624942 | ||||||
| chr6:106624946
|
A | AAAAAAG | 35 | a0001c0002t0005g0001a0001c0002t0005g0324a0001c0002t0005g0325others(32): Show | 39 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.275-1983_275-1978d others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624946 | ||||||
| chr6:106624946
|
A | AAAAAAGA others(5): Show |
1 | a0001c0002t0005g0323 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.275-1989_275-1978d others(14): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624946 | ||||||
| chr6:106624946
|
AAAAAAG | A | 59 | a0001c0003t0004g0012a0001c0003t0004g0143a0001c0003t0004g0154others(56): Show | 68 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.275-1983_275-1978d others(8): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624946 | ||||||
| chr6:106624946
|
AAAAAAGA others(5): Show |
A | 3 | a0001c0001t0002g0047a0001c0003t0004g0221a0001c0003t0004g0223 | 3 | HG01192.hp2 HG02055.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.275-1989_275-1978d others(14): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624946 | ||||||
| chr6:106624947
|
AAAAAG | A | 14 | a0001c0004t0003g0096a0001c0004t0003g0097a0001c0004t0003g0099others(11): Show | 14 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.275-1983_275-1979d others(7): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106624947 | ||||||
| chr6:106625035
|
C | T | 3 | a0001c0001t0001g0238a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG02572.hp2 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.275-2066G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625035 | ||||||
| chr6:106625198
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.275-2229C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625198 | ||||||
| chr6:106625264
|
C | A | 1 | a0001c0005t0009g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.275-2295G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625264 | ||||||
| chr6:106625290
|
C | T | 1 | a0001c0003t0004g0154 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.275-2321G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625290 | ||||||
| chr6:106625388
|
C | T | 3 | a0001c0004t0003g0096a0001c0004t0003g0097a0001c0004t0003g0099 | 3 | HG01175.hp1 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.275-2419G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625388 | ||||||
| chr6:106625389
|
G | A | 7 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0257others(4): Show | 7 | HG02258.hp1 HG02717.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-2420C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625389 | ||||||
| chr6:106625524
|
T | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-2555A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625524 | ||||||
| chr6:106625535
|
A | T | 54 | a0001c0003t0004g0012a0001c0003t0004g0014a0001c0003t0004g0015others(51): Show | 57 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.275-2566T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625535 | ||||||
| chr6:106625614
|
G | A | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.275-2645C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625614 | ||||||
| chr6:106625627
|
C | T | 1 | a0001c0004t0003g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.275-2658G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625627 | ||||||
| chr6:106625645
|
C | T | 2 | a0001c0004t0003g0096a0001c0004t0003g0097 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.275-2676G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625645 | ||||||
| chr6:106625661
|
C | CT | 78 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0258others(75): Show | 85 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.275-2693dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625661 | ||||||
| chr6:106625665
|
T | TC | 54 | a0001c0003t0004g0205a0001c0004t0003g0002a0001c0004t0003g0003others(51): Show | 62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.275-2697_275-2696i others(3): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625665 | ||||||
| chr6:106625732
|
C | G | 54 | a0001c0003t0004g0205a0001c0004t0003g0002a0001c0004t0003g0003others(51): Show | 62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.275-2763G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625732 | ||||||
| chr6:106625750
|
G | A | 1 | a0001c0005t0009g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.275-2781C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625750 | ||||||
| chr6:106625813
|
G | A | 1 | a0001c0002t0010g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.275-2844C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625813 | ||||||
| chr6:106625868
|
A | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+2880T>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625868 | ||||||
| chr6:106625908
|
G | A | 2 | a0001c0002t0005g0353a0001c0002t0005g0354 | 2 | NA18952.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.274+2840C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625908 | ||||||
| chr6:106625996
|
G | A | 2 | a0001c0003t0014g0017a0003c0012t0002g0091 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.274+2752C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106625996 | ||||||
| chr6:106626008
|
A | G | 57 | a0001c0003t0004g0205a0001c0003t0014g0017a0001c0004t0003g0002others(54): Show | 65 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.274+2740T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626008 | ||||||
| chr6:106626064
|
T | C | 32 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(29): Show | 34 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.274+2684A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626064 | ||||||
| chr6:106626135
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.274+2613G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626135 | ||||||
| chr6:106626161
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.274+2587C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626161 | ||||||
| chr6:106626238
|
T | C | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.274+2510A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626238 | ||||||
| chr6:106626341
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.274+2407G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626341 | ||||||
| chr6:106626344
|
T | C | 1 | a0001c0002t0005g0355 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.274+2404A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626344 | ||||||
| chr6:106626383
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.274+2365T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626383 | ||||||
| chr6:106626591
|
C | T | 1 | a0005c0010t0013g0018 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.274+2157G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626591 | ||||||
| chr6:106626592
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.274+2156A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626592 | ||||||
| chr6:106626730
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.274+2018C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626730 | ||||||
| chr6:106626946
|
G | A | 55 | a0001c0003t0014g0017a0001c0004t0003g0002a0001c0004t0003g0003others(52): Show | 63 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.274+1802C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626946 | ||||||
| chr6:106626983
|
C | A | 1 | a0001c0004t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.274+1765G>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106626983 | ||||||
| chr6:106627141
|
G | GA | 370 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0232others(367): Show | 394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.274+1606dupT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627141 | ||||||
| chr6:106627310
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0235a0001c0001t0001g0254others(2): Show | 7 | NA18952.hp2 NA18978.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.274+1438G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627310 | ||||||
| chr6:106627389
|
T | C | 2 | a0001c0004t0003g0139a0001c0005t0009g0138 | 2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.274+1359A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627389 | ||||||
| chr6:106627574
|
A | G | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+1174T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627574 | ||||||
| chr6:106627696
|
T | C | 87 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0160others(84): Show | 92 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+1052A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627696 | ||||||
| chr6:106627702
|
C | T | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+1046G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627702 | ||||||
| chr6:106627743
|
C | CT | 85 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(82): Show | 87 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.274+1004dupA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | ||||||
| chr6:106627743
|
C | CTT | 52 | a0001c0001t0001g0234a0001c0001t0002g0020a0001c0001t0006g0362others(49): Show | 56 | HG00438.hp2 HG00738.hp1 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.274+1003_274+1004d others(4): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | ||||||
| chr6:106627743
|
C | CTTT | 14 | a0001c0002t0001g0160a0001c0002t0001g0161a0001c0002t0001g0162others(11): Show | 14 | HG01070.hp2 HG01433.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+1002_274+1004d others(5): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | ||||||
| chr6:106627743
|
C | CTTTTTTT others(5): Show |
1 | a0001c0002t0001g0011 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.274+993_274+1004du others(13): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | ||||||
| chr6:106627743
|
CT | C | 12 | a0001c0001t0002g0090a0001c0002t0005g0357a0001c0002t0010g0359others(9): Show | 12 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.274+1004delA | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | ||||||
| chr6:106627743
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0004t0003g0093a0001c0005t0009g0094a0001c0005t0009g0095 | 3 | HG02615.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.274+995_274+1004de others(11): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | ||||||
| chr6:106627743
|
CTTTTTTT others(4): Show |
C | 49 | a0001c0004t0003g0002a0001c0004t0003g0003a0001c0004t0003g0004others(46): Show | 57 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.274+994_274+1004de others(12): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | ||||||
| chr6:106627743
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0003g0140 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.274+993_274+1004de others(13): Show |
RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627743 | ||||||
| chr6:106627776
|
T | C | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+972A>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627776 | ||||||
| chr6:106627805
|
T | A | 1 | a0001c0002t0010g0361 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274+943A>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627805 | ||||||
| chr6:106627884
|
A | G | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.274+864T>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106627884 | ||||||
| chr6:106628025
|
G | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+723C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628025 | ||||||
| chr6:106628050
|
G | C | 1 | a0001c0002t0001g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.274+698C>G | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628050 | ||||||
| chr6:106628146
|
A | T | 1 | a0001c0008t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+602T>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628146 | ||||||
| chr6:106628219
|
G | A | 9 | a0001c0003t0007g0144a0001c0003t0007g0145a0001c0003t0007g0146others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+529C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628219 | ||||||
| chr6:106628222
|
C | G | 1 | a0001c0004t0003g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.274+526G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628222 | ||||||
| chr6:106628237
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.274+511G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628237 | ||||||
| chr6:106628258
|
G | A | 1 | a0001c0003t0014g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.274+490C>T | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628258 | ||||||
| chr6:106628467
|
CA | C | 10 | a0001c0003t0004g0143a0001c0003t0007g0144a0001c0003t0007g0145others(7): Show | 10 | HG02257.hp1 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+280delT | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628467 | ||||||
| chr6:106628501
|
C | G | 1 | a0001c0003t0004g0142 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.274+247G>C | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628501 | ||||||
| chr6:106628562
|
C | T | 1 | a0001c0002t0001g0010 | 2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.274+186G>A | RTN4IP1 | ENSG00000130347.13 | transcript | ENST00000369063.8 | protein_coding | 1/8 | chr6 | 106628562 |