| geneid | 57142 |
|---|---|
| ensemblid | ENSG00000115310.19 |
| hgncid | 14085 |
| symbol | RTN4 |
| name | reticulon 4 |
| refseq_nuc | NM_020532.5 |
| refseq_prot | NP_065393.1 |
| ensembl_nuc | ENST00000337526.11 |
| ensembl_prot | ENSP00000337838.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 54972189 |
| end | 55050451 |
| strand | - |
| ver | v1.2 |
| region | chr2:54972189-55050451 |
| region5000 | chr2:54967189-55055451 |
| regionname0 | RTN4_chr2_54972189_55050451 |
| regionname5000 | RTN4_chr2_54967189_55055451 |
| 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 | 1192 | 254 | 65 | 35 | 110 | 13 | 29 | 92 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0002 | 0/0 | 1192 | 49 | 1 | 18 | 21 | 1 | 8 | 17 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0003 | 0/0 | 1192 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0004 | 0/0 | 1192 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0005 | 0/0 | 1192 | 8 | 0 | 2 | 5 | 1 | 0 | 4 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0006 | 0/0 | 1192 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0007 | 0/0 | 1192 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0008 | 0/0 | 1192 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0009 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0010 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0011 | 0/0 | 1192 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0012 | 0/0 | 1192 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0013 | 0/0 | 1192 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0014 | 0/0 | 1192 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0015 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0016 | 0/0 | 1192 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0017 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| 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 | 3579 | 243 | 59 | 31 | 109 | 13 | 29 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0002 | 0/0 | 3579 | 48 | 1 | 17 | 21 | 1 | 8 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0003 | 0/0 | 3579 | 9 | 9 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0004 | 0/0 | 3579 | 8 | 0 | 2 | 5 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0005 | 0/0 | 3579 | 8 | 8 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0006 | 0/0 | 3579 | 6 | 5 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0007 | 0/0 | 3579 | 5 | 4 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0008 | 0/0 | 3579 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0009 | 0/0 | 3579 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0010 | 0/0 | 3579 | 2 | 0 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0011 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0012 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0013 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0014 | 0/0 | 3579 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0015 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0016 | 0/0 | 3579 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0017 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0018 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0019 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0020 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0021 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0022 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0023 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0024 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| c0025 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| 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 | 1/0 | 1119 | 111 | 19 | 18 | 53 | 8 | 12 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0002 | 0/1 | 1118 | 97 | 8 | 16 | 61 | 6 | 5 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0003 | 0/0 | 1120 | 44 | 1 | 17 | 19 | 1 | 6 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0004 | 0/0 | 1120 | 28 | 26 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0005 | 0/0 | 1115 | 26 | 13 | 3 | 0 | 1 | 9 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0006 | 0/0 | 1115 | 5 | 5 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0007 | 0/0 | 1120 | 5 | 5 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0008 | 0/0 | 1120 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0009 | 0/0 | 1120 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0010 | 0/0 | 1124 | 3 | 1 | 0 | 0 | 0 | 2 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0011 | 0/0 | 1124 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0012 | 0/0 | 1122 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0013 | 0/0 | 1119 | 3 | 2 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0014 | 0/0 | 1120 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0015 | 0/0 | 1118 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0016 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0017 | 0/0 | 1120 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0018 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0019 | 0/0 | 1120 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0020 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0021 | 0/0 | 1123 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0022 | 0/0 | 1119 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0023 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0024 | 0/0 | 1118 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| t0025 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| 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 | 3 | 0 | 1 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| 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 | 3579 | 243 | 59 | 31 | 109 | 13 | 29 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0008 | 0/0 | 3579 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0010 | 0/0 | 3579 | 2 | 0 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0012 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0013 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0017 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0021 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0023 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0002c0002 | 0/0 | 3579 | 48 | 1 | 17 | 21 | 1 | 8 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0002c0011 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0003c0003 | 0/0 | 3579 | 9 | 9 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0004c0005 | 0/0 | 3579 | 8 | 8 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0005c0004 | 0/0 | 3579 | 8 | 0 | 2 | 5 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0006c0006 | 0/0 | 3579 | 6 | 5 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0007c0007 | 0/0 | 3579 | 5 | 4 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0008c0009 | 0/0 | 3579 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0009c0025 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0010c0024 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0011c0022 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0012c0014 | 0/0 | 3579 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0013c0019 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0014c0018 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0015c0020 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0016c0016 | 0/0 | 3579 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0017c0015 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4697 | 92 | 11 | 14 | 49 | 7 | 10 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0002 | 0/1 | 4696 | 77 | 3 | 11 | 52 | 5 | 5 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0003 | 0/0 | 4698 | 5 | 0 | 0 | 5 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0004 | 0/0 | 4698 | 17 | 15 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0005 | 0/0 | 4693 | 26 | 13 | 3 | 0 | 1 | 9 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0006 | 0/0 | 4693 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0007 | 0/0 | 4698 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0009 | 0/0 | 4698 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0010 | 0/0 | 4702 | 3 | 1 | 0 | 0 | 0 | 2 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0012 | 0/0 | 4700 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0013 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0015 | 0/0 | 4696 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0017 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0021 | 0/0 | 4701 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0022 | 0/0 | 4697 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0024 | 0/0 | 4696 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0001t0025 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0008t0008 | 0/0 | 4698 | 3 | 3 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0008t0018 | 0/0 | 4700 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0010t0002 | 0/0 | 4696 | 2 | 0 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0012t0004 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0013t0001 | 0/0 | 4697 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0017t0001 | 0/0 | 4697 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0021t0007 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0001c0023t0001 | 0/0 | 4697 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0002c0002t0001 | 0/0 | 4697 | 2 | 0 | 1 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0002c0002t0002 | 0/0 | 4696 | 4 | 0 | 0 | 4 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0002c0002t0003 | 0/0 | 4698 | 38 | 1 | 16 | 14 | 1 | 6 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0002c0002t0011 | 0/0 | 4702 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0002c0002t0019 | 0/0 | 4698 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0002c0011t0003 | 0/0 | 4698 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0003c0003t0004 | 0/0 | 4698 | 7 | 7 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0003c0003t0014 | 0/0 | 4698 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0004c0005t0001 | 0/0 | 4697 | 8 | 8 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0005c0004t0002 | 0/0 | 4696 | 8 | 0 | 2 | 5 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0006c0006t0002 | 0/0 | 4696 | 5 | 4 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0006c0006t0023 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0007c0007t0004 | 0/0 | 4698 | 3 | 3 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0007c0007t0013 | 0/0 | 4697 | 2 | 1 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0008c0009t0001 | 0/0 | 4697 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0009c0025t0016 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0010c0024t0006 | 0/0 | 4693 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0011c0022t0001 | 0/0 | 4697 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0012c0014t0001 | 0/0 | 4697 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0013c0019t0001 | 0/0 | 4697 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0014c0018t0020 | 0/0 | 4700 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0015c0020t0002 | 0/0 | 4696 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0016c0016t0001 | 0/0 | 4697 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| a0017c0015t0008 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | copy fasta | chr2 | 54967189 | 55055451 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0009g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0010g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0010g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0012g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0012g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0012g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0015g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0015g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0017g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0021g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0022g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0024g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0001t0025g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0008t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0008t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0008t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0008t0018g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0010t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0010t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0012t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0013t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0017t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0021t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0001c0023t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0011g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0002t0019g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0002c0011t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0003c0003t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0003c0003t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0003c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0003c0003t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0003c0003t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0003c0003t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0003c0003t0014g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0004c0005t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0004c0005t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0004c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0004c0005t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0004c0005t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0004c0005t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0004c0005t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0004c0005t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0005c0004t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0005c0004t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0005c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0005c0004t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0005c0004t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0005c0004t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0005c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0006c0006t0002g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0006c0006t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0006c0006t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0006c0006t0023g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0007c0007t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0007c0007t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0007c0007t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0007c0007t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0007c0007t0013g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0008c0009t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0008c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0009c0025t0016g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0010c0024t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0011c0022t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0012c0014t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0013c0019t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0014c0018t0020g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0015c0020t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0016c0016t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| a0017c0015t0008g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0290 | EUR | GBR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0274 | EUR | GBR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | GBR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | FIN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00544 | hp2 | a0002 | c0002 | t0003 | g0020 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00558 | hp2 | a0008 | c0009 | t0001 | g0106 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00642 | hp1 | a0002 | c0002 | t0003 | g0054 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0041 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00738 | hp1 | a0006 | c0006 | t0002 | g0003 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0038 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0288 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01070 | hp1 | a0002 | c0002 | t0003 | g0051 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01070 | hp2 | a0005 | c0004 | t0002 | g0009 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0287 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01071 | hp2 | a0005 | c0004 | t0002 | g0009 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01074 | hp2 | a0002 | c0002 | t0003 | g0014 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01167 | hp1 | a0007 | c0007 | t0013 | g0065 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01167 | hp2 | a0002 | c0002 | t0003 | g0061 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01168 | hp2 | a0002 | c0002 | t0003 | g0035 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01256 | hp1 | a0001 | c0010 | t0002 | g0320 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0013 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01257 | hp2 | a0011 | c0022 | t0001 | g0319 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01258 | hp1 | a0001 | c0010 | t0002 | g0321 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01258 | hp2 | a0002 | c0002 | t0003 | g0017 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0048 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01496 | hp1 | a0001 | c0017 | t0001 | g0265 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0015 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01515 | hp1 | a0005 | c0004 | t0002 | g0137 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01516 | hp1 | a0002 | c0002 | t0003 | g0024 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0166 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0304 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01884 | hp2 | a0001 | c0001 | t0025 | g0080 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01891 | hp2 | a0003 | c0003 | t0004 | g0004 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01943 | hp2 | a0002 | c0011 | t0003 | g0046 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01952 | hp1 | a0001 | c0001 | t0024 | g0154 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01952 | hp2 | a0002 | c0002 | t0003 | g0016 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0036 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0039 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0119 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02132 | hp2 | a0001 | c0001 | t0012 | g0267 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0276 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0310 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0032 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CDX | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0303 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0040 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0042 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02451 | hp2 | a0007 | c0007 | t0004 | g0066 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02523 | hp1 | a0002 | c0002 | t0003 | g0021 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02523 | hp2 | a0005 | c0004 | t0002 | g0191 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02572 | hp1 | a0003 | c0003 | t0004 | g0073 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02615 | hp1 | a0010 | c0024 | t0006 | g0331 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0299 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0333 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02683 | hp1 | a0002 | c0002 | t0003 | g0050 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0289 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02698 | hp2 | a0002 | c0002 | t0003 | g0031 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02717 | hp2 | a0003 | c0003 | t0004 | g0005 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02723 | hp1 | a0004 | c0005 | t0001 | g0330 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0082 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0286 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02809 | hp1 | a0001 | c0008 | t0018 | g0067 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0298 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02818 | hp1 | a0004 | c0005 | t0001 | g0325 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02818 | hp2 | a0001 | c0008 | t0008 | g0261 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02886 | hp1 | a0006 | c0006 | t0002 | g0003 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02886 | hp2 | a0001 | c0008 | t0008 | g0259 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02895 | hp1 | a0003 | c0003 | t0004 | g0318 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02895 | hp2 | a0017 | c0015 | t0008 | g0308 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02896 | hp1 | a0004 | c0005 | t0001 | g0324 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0316 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02897 | hp1 | a0004 | c0005 | t0001 | g0326 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02897 | hp2 | a0003 | c0003 | t0004 | g0317 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02922 | hp1 | a0006 | c0006 | t0002 | g0302 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02922 | hp2 | a0003 | c0003 | t0004 | g0005 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0309 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02970 | hp2 | a0001 | c0021 | t0007 | g0336 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0296 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0055 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03130 | hp2 | a0007 | c0007 | t0004 | g0062 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0149 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0313 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03209 | hp2 | a0003 | c0003 | t0004 | g0004 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03225 | hp2 | a0004 | c0005 | t0001 | g0329 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0057 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03453 | hp1 | a0006 | c0006 | t0002 | g0003 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0293 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0335 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03486 | hp2 | a0001 | c0008 | t0008 | g0260 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03491 | hp2 | a0002 | c0002 | t0019 | g0023 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0011 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03516 | hp1 | a0015 | c0020 | t0002 | g0315 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03516 | hp2 | a0003 | c0003 | t0014 | g0071 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03540 | hp2 | a0004 | c0005 | t0001 | g0327 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0334 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03654 | hp1 | a0001 | c0001 | t0015 | g0254 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0285 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0282 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0283 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0052 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03710 | hp1 | a0001 | c0001 | t0022 | g0221 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0049 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03834 | hp2 | a0001 | c0001 | t0010 | g0275 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0281 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03927 | hp2 | a0001 | c0001 | t0010 | g0273 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG04184 | hp1 | a0001 | c0001 | t0015 | g0145 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG04184 | hp2 | a0002 | c0002 | t0003 | g0053 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG04228 | hp2 | a0012 | c0014 | t0001 | g0244 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18522 | hp2 | a0006 | c0006 | t0002 | g0301 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18952 | hp1 | a0002 | c0002 | t0003 | g0027 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0028 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18972 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18974 | hp1 | a0005 | c0004 | t0002 | g0170 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18985 | hp1 | a0014 | c0018 | t0020 | g0164 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18985 | hp2 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18986 | hp1 | a0001 | c0001 | t0012 | g0264 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18987 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18989 | hp2 | a0002 | c0002 | t0003 | g0037 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18990 | hp2 | a0005 | c0004 | t0002 | g0168 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18992 | hp1 | a0002 | c0002 | t0011 | g0018 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18993 | hp2 | a0002 | c0002 | t0011 | g0043 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18999 | hp1 | a0001 | c0001 | t0012 | g0268 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19003 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0295 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19030 | hp2 | a0009 | c0025 | t0016 | g0012 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19055 | hp2 | a0001 | c0023 | t0001 | g0322 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19056 | hp1 | a0013 | c0019 | t0001 | g0269 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19057 | hp1 | a0005 | c0004 | t0002 | g0167 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19058 | hp1 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19064 | hp2 | a0002 | c0002 | t0003 | g0033 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19082 | hp1 | a0008 | c0009 | t0001 | g0105 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19082 | hp2 | a0002 | c0002 | t0011 | g0034 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19086 | hp1 | a0005 | c0004 | t0002 | g0169 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA19240 | hp2 | a0004 | c0005 | t0001 | g0328 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20129 | hp1 | a0001 | c0012 | t0004 | g0213 | AFR | ASW | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0332 | AFR | ASW | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20752 | hp2 | a0016 | c0016 | t0001 | g0107 | EUR | TSI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0284 | SAS | GIH | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | GIH | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01123 | hp1 | a0001 | c0013 | t0001 | g0122 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0291 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02109 | hp1 | a0004 | c0005 | t0001 | g0323 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02559 | hp1 | a0007 | c0007 | t0004 | g0063 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0192 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG03471 | hp2 | a0006 | c0006 | t0023 | g0305 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG06807 | hp1 | a0007 | c0007 | t0013 | g0064 | AFR | USA | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | USA | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0068 | AFR | USA | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA21309 | hp1 | a0003 | c0003 | t0014 | g0072 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0183 | REF | REF | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0253 | REF | REF | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:54973197
|
T | A | 1 | a0014 | 1 | NA18985.hp1 | missense_variant&splice_region_variant | MODERATE | c.3538A>T | p.Ile1180Phe | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 3689/4697 | 3538/3579 | 1180/1192 | chr2 | 54973197 | ||
| chr2:54982570
|
G | A | 1 | a0013 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.3305C>T | p.Thr1102Met | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/9 | 3456/4697 | 3305/3579 | 1102/1192 | chr2 | 54982570 | ||
| chr2:54982630
|
G | C | 1 | a0015 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.3245C>G | p.Ala1082Gly | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/9 | 3396/4697 | 3245/3579 | 1082/1192 | chr2 | 54982630 | ||
| chr2:55025328
|
A | G | 1 | a0006 | 6 | HG00738.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
missense_variant | MODERATE | c.2771T>C | p.Ile924Thr | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2922/4697 | 2771/3579 | 924/1192 | chr2 | 55025328 | ||
| chr2:55025340
|
G | C | 1 | a0003 | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
missense_variant | MODERATE | c.2759C>G | p.Ser920Cys | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2910/4697 | 2759/3579 | 920/1192 | chr2 | 55025340 | ||
| chr2:55025404
|
C | G | 1 | a0003 | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
missense_variant | MODERATE | c.2695G>C | p.Glu899Gln | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2846/4697 | 2695/3579 | 899/1192 | chr2 | 55025404 | ||
| chr2:55025659
|
G | T | 1 | a0016 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2440C>A | p.Leu814Met | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2591/4697 | 2440/3579 | 814/1192 | chr2 | 55025659 | ||
| chr2:55025743
|
C | T | 1 | a0017 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.2356G>A | p.Glu786Lys | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2507/4697 | 2356/3579 | 786/1192 | chr2 | 55025743 | ||
| chr2:55025808
|
A | T | 1 | a0012 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.2291T>A | p.Val764Glu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2442/4697 | 2291/3579 | 764/1192 | chr2 | 55025808 | ||
| chr2:55026750
|
G | A | 2 | a0004a0009 | 9 | HG02109.hp1 HG02723.hp1 HG02818.hp1 others(6): Show |
missense_variant | MODERATE | c.1349C>T | p.Thr450Met | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1500/4697 | 1349/3579 | 450/1192 | chr2 | 55026750 | ||
| chr2:55026924
|
C | T | 1 | a0007 | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
missense_variant | MODERATE | c.1175G>A | p.Arg392Gln | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1326/4697 | 1175/3579 | 392/1192 | chr2 | 55026924 | ||
| chr2:55026960
|
A | G | 1 | a0008 | 2 | HG00558.hp2 NA19082.hp1 |
missense_variant | MODERATE | c.1139T>C | p.Met380Thr | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1290/4697 | 1139/3579 | 380/1192 | chr2 | 55026960 | ||
| chr2:55027029
|
T | A | 1 | a0005 | 8 | HG01070.hp2 HG01071.hp2 HG01515.hp1 others(5): Show |
missense_variant | MODERATE | c.1070A>T | p.Asp357Val | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1221/4697 | 1070/3579 | 357/1192 | chr2 | 55027029 | ||
| chr2:55049968
|
G | C | 1 | a0011 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.333C>G | p.Ser111Arg | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 484/4697 | 333/3579 | 111/1192 | chr2 | 55049968 | ||
| chr2:55050072
|
G | C | 3 | a0004a0009a0010 | 10 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(7): Show |
missense_variant | MODERATE | c.229C>G | p.Pro77Ala | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 380/4697 | 229/3579 | 77/1192 | chr2 | 55050072 | ||
| chr2:55050090
|
C | T | 1 | a0002 | 49 | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(46): Show |
missense_variant | MODERATE | c.211G>A | p.Ala71Thr | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 362/4697 | 211/3579 | 71/1192 | chr2 | 55050090 | ||
| chr2:55050178
|
T | G | 1 | a0010 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.123A>C | p.Glu41Asp | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 274/4697 | 123/3579 | 41/1192 | chr2 | 55050178 | ||
| chr2:55050282
|
A | T | 1 | a0009 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.19T>A | p.Ser7Thr | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 170/4697 | 19/3579 | 7/1192 | chr2 | 55050282 | ||
| chr2:55050285
|
G | C | 1 | a0009 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.16C>G | p.Gln6Glu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 167/4697 | 16/3579 | 6/1192 | chr2 | 55050285 | ||
| chr2:55050290
|
A | C | 1 | a0009 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.11T>G | p.Leu4Arg | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 162/4697 | 11/3579 | 4/1192 | chr2 | 55050290 | ||
| chr2:55050293
|
T | C | 1 | a0009 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.8A>G | p.Asp3Gly | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 159/4697 | 8/3579 | 3/1192 | chr2 | 55050293 | ||
| chr2:55050296
|
T | A | 1 | a0009 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.5A>T | p.Glu2Val | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 156/4697 | 5/3579 | 2/1192 | chr2 | 55050296 | ||
| chr2:55050299
|
A | C | 1 | a0009 | 1 | NA19030.hp2 | start_lost | HIGH | c.2T>G | p.Met1? | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 153/4697 | 2/3579 | 1/1192 | chr2 | 55050299 | ||
| chr2:55050300
|
T | C | 1 | a0009 | 1 | NA19030.hp2 | start_lost | HIGH | c.1A>G | p.Met1? | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 152/4697 | 1/3579 | 1/1192 | chr2 | 55050300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:55025123
|
T | C | 2 | a0001c0008a0017c0015 | 5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.2976A>G | p.Pro992Pro | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 3127/4697 | 2976/3579 | 992/1192 | chr2 | 55025123 | ||
| chr2:55025330
|
G | A | 1 | a0001c0021 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2769C>T | p.Asn923Asn | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2920/4697 | 2769/3579 | 923/1192 | chr2 | 55025330 | ||
| chr2:55025387
|
C | T | 1 | a0001c0017 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.2712G>A | p.Pro904Pro | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2863/4697 | 2712/3579 | 904/1192 | chr2 | 55025387 | ||
| chr2:55025408
|
T | C | 1 | a0002c0011 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.2691A>G | p.Lys897Lys | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2842/4697 | 2691/3579 | 897/1192 | chr2 | 55025408 | ||
| chr2:55026241
|
A | G | 2 | a0001c0012a0007c0007 | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
synonymous_variant | LOW | c.1858T>C | p.Leu620Leu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2009/4697 | 1858/3579 | 620/1192 | chr2 | 55026241 | ||
| chr2:55026911
|
C | T | 1 | a0001c0013 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.1188G>A | p.Val396Val | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1339/4697 | 1188/3579 | 396/1192 | chr2 | 55026911 | ||
| chr2:55028219
|
A | G | 1 | a0001c0012 | 1 | NA20129.hp1 | splice_region_variant&synonymous_variant | LOW | c.558T>C | p.Asp186Asp | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/9 | 709/4697 | 558/3579 | 186/1192 | chr2 | 55028219 | ||
| chr2:55050007
|
G | C | 1 | a0001c0010 | 2 | HG01256.hp1 HG01258.hp1 |
synonymous_variant | LOW | c.294C>G | p.Pro98Pro | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 445/4697 | 294/3579 | 98/1192 | chr2 | 55050007 | ||
| chr2:55050034
|
C | A | 1 | a0001c0023 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.267G>T | p.Ala89Ala | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 418/4697 | 267/3579 | 89/1192 | chr2 | 55050034 | ||
| chr2:55050280
|
A | G | 1 | a0009c0025 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.21T>C | p.Ser7Ser | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 172/4697 | 21/3579 | 7/1192 | chr2 | 55050280 | ||
| chr2:55050291
|
G | A | 1 | a0009c0025 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.10C>T | p.Leu4Leu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 161/4697 | 10/3579 | 4/1192 | chr2 | 55050291 | ||
| chr2:55050295
|
T | C | 1 | a0009c0025 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.6A>G | p.Glu2Glu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 157/4697 | 6/3579 | 2/1192 | chr2 | 55050295 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:54972306
|
T | A | 8 | a0001c0001t0004a0001c0001t0013a0001c0001t0017others(5): Show | 34 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*850A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 850 | chr2 | 54972306 | |||||
| chr2:54972320
|
A | ATGTT | 2 | a0001c0001t0021a0002c0002t0011 | 4 | HG02055.hp2 NA18992.hp1 NA18993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*832_*835dupAACA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 835 | chr2 | 54972320 | |||||
| chr2:54972363
|
A | G | 1 | a0001c0008t0018 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 793 | chr2 | 54972363 | |||||
| chr2:54972374
|
A | C | 3 | a0001c0001t0007a0001c0001t0009a0001c0021t0007 | 9 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*782T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 782 | chr2 | 54972374 | |||||
| chr2:54972380
|
T | A | 1 | a0014c0018t0020 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*776A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 776 | chr2 | 54972380 | |||||
| chr2:54972421
|
A | ATGT | 12 | a0001c0001t0002a0001c0001t0012a0001c0001t0015others(9): Show | 106 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*732_*734dupACA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 734 | chr2 | 54972421 | |||||
| chr2:54972464
|
T | C | 1 | a0001c0001t0022 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*692A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 692 | chr2 | 54972464 | |||||
| chr2:54972628
|
T | C | 3 | a0001c0008t0008a0001c0008t0018a0017c0015t0008 | 5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*528A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 528 | chr2 | 54972628 | |||||
| chr2:54972707
|
C | T | 1 | a0002c0002t0019 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*449G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 449 | chr2 | 54972707 | |||||
| chr2:54972712
|
T | C | 2 | a0001c0001t0006a0010c0024t0006 | 5 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*444A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 444 | chr2 | 54972712 | |||||
| chr2:54972795
|
C | CT | 17 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(14): Show | 93 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*360dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 360 | chr2 | 54972795 | |||||
| chr2:54972819
|
C | A | 1 | a0001c0001t0024 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 337 | chr2 | 54972819 | |||||
| chr2:54972902
|
CAGAT | C | 12 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(9): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*250_*253delATCT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 250 | chr2 | 54972902 | |||||
| chr2:54972905
|
A | ATAGAT | 1 | a0001c0001t0010 | 3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*246_*250dupATCTA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 250 | chr2 | 54972905 | |||||
| chr2:54972929
|
C | A | 1 | a0001c0001t0025 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*227G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 227 | chr2 | 54972929 | |||||
| chr2:54972945
|
A | G | 3 | a0001c0008t0008a0001c0008t0018a0017c0015t0008 | 5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*211T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 211 | chr2 | 54972945 | |||||
| chr2:54972968
|
T | A | 1 | a0003c0003t0014 | 2 | HG03516.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*188A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 188 | chr2 | 54972968 | |||||
| chr2:54972986
|
C | A | 1 | a0001c0001t0017 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*170G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 170 | chr2 | 54972986 | |||||
| chr2:54972989
|
G | T | 1 | a0001c0001t0017 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 167 | chr2 | 54972989 | |||||
| chr2:54973086
|
G | C | 1 | a0001c0001t0015 | 2 | HG03654.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*70C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 70 | chr2 | 54973086 | |||||
| chr2:55050304
|
T | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 4 | chr2 | 55050304 | |||||
| chr2:55050306
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050306 | ||||||
| chr2:55050310
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 10 | chr2 | 55050310 | |||||
| chr2:55050311
|
T | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 11 | chr2 | 55050311 | |||||
| chr2:55050312
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-12C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 12 | chr2 | 55050312 | |||||
| chr2:55050314
|
A | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-14T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 14 | chr2 | 55050314 | |||||
| chr2:55050316
|
A | T | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-16T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 16 | chr2 | 55050316 | |||||
| chr2:55050318
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050318 | ||||||
| chr2:55050320
|
T | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 20 | chr2 | 55050320 | |||||
| chr2:55050322
|
C | T | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-22G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 22 | chr2 | 55050322 | |||||
| chr2:55050323
|
T | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-23A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050323 | ||||||
| chr2:55050324
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 24 | chr2 | 55050324 | |||||
| chr2:55050328
|
C | T | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-28G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 28 | chr2 | 55050328 | |||||
| chr2:55050330
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 30 | chr2 | 55050330 | |||||
| chr2:55050331
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-31G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 31 | chr2 | 55050331 | |||||
| chr2:55050334
|
C | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-34G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 34 | chr2 | 55050334 | |||||
| chr2:55050335
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-35G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 35 | chr2 | 55050335 | |||||
| chr2:55050337
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 37 | chr2 | 55050337 | |||||
| chr2:55050338
|
C | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050338 | ||||||
| chr2:55050346
|
G | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 46 | chr2 | 55050346 | |||||
| chr2:55050349
|
C | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 49 | chr2 | 55050349 | |||||
| chr2:55050352
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-52G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 52 | chr2 | 55050352 | |||||
| chr2:55050354
|
T | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 54 | chr2 | 55050354 | |||||
| chr2:55050355
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 55 | chr2 | 55050355 | |||||
| chr2:55050356
|
T | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 56 | chr2 | 55050356 | |||||
| chr2:55050357
|
C | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-57G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 57 | chr2 | 55050357 | |||||
| chr2:55050361
|
G | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 61 | chr2 | 55050361 | |||||
| chr2:55050362
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 62 | chr2 | 55050362 | |||||
| chr2:55050363
|
C | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050363 | ||||||
| chr2:55050365
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 65 | chr2 | 55050365 | |||||
| chr2:55050366
|
G | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050366 | ||||||
| chr2:55050369
|
C | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-69G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 69 | chr2 | 55050369 | |||||
| chr2:55050372
|
T | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 72 | chr2 | 55050372 | |||||
| chr2:55050373
|
T | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-73A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 73 | chr2 | 55050373 | |||||
| chr2:55050375
|
T | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 75 | chr2 | 55050375 | |||||
| chr2:55050378
|
G | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-78C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 78 | chr2 | 55050378 | |||||
| chr2:55050381
|
T | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 81 | chr2 | 55050381 | |||||
| chr2:55050382
|
T | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 82 | chr2 | 55050382 | |||||
| chr2:55050384
|
G | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 84 | chr2 | 55050384 | |||||
| chr2:55050388
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-88C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 88 | chr2 | 55050388 | |||||
| chr2:55050399
|
G | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-99C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 99 | chr2 | 55050399 | |||||
| chr2:55050401
|
C | A | 2 | a0001c0001t0007a0001c0021t0007 | 5 | HG02647.hp2 HG02970.hp2 HG03486.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-101G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 101 | chr2 | 55050401 | |||||
| chr2:55050406
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 106 | chr2 | 55050406 | |||||
| chr2:55050407
|
C | T | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-107G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 107 | chr2 | 55050407 | |||||
| chr2:55050409
|
A | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-109T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 109 | chr2 | 55050409 | |||||
| chr2:55050410
|
C | T | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 110 | chr2 | 55050410 | |||||
| chr2:55050411
|
T | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-111A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 111 | chr2 | 55050411 | |||||
| chr2:55050415
|
C | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-115G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 115 | chr2 | 55050415 | |||||
| chr2:55050416
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-116G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 116 | chr2 | 55050416 | |||||
| chr2:55050419
|
G | A | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-119C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 119 | chr2 | 55050419 | |||||
| chr2:55050421
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 121 | chr2 | 55050421 | |||||
| chr2:55050422
|
A | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-122T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 122 | chr2 | 55050422 | |||||
| chr2:55050425
|
T | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 125 | chr2 | 55050425 | |||||
| chr2:55050426
|
A | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-126T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 126 | chr2 | 55050426 | |||||
| chr2:55050428
|
T | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 128 | chr2 | 55050428 | |||||
| chr2:55050430
|
T | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 130 | chr2 | 55050430 | |||||
| chr2:55050432
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 132 | chr2 | 55050432 | |||||
| chr2:55050435
|
A | T | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 135 | chr2 | 55050435 | |||||
| chr2:55050437
|
G | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 137 | chr2 | 55050437 | |||||
| chr2:55050440
|
T | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-140A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 140 | chr2 | 55050440 | |||||
| chr2:55050441
|
C | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 141 | chr2 | 55050441 | |||||
| chr2:55050447
|
A | C | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 147 | chr2 | 55050447 | |||||
| chr2:55050450
|
A | G | 1 | a0009c0025t0016 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-150T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:54973648
|
T | G | 1 | a0001c0001t0001g0249 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3478-27A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 7/8 | chr2 | 54973648 | ||||||
| chr2:54973664
|
T | G | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(88): Show | 100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.3478-43A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 7/8 | chr2 | 54973664 | ||||||
| chr2:54973759
|
G | A | 1 | a0001c0001t0024g0154 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3477+62C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 7/8 | chr2 | 54973759 | ||||||
| chr2:54973902
|
C | T | 249 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(246): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.3431-35G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54973902 | ||||||
| chr2:54973980
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3431-113T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54973980 | ||||||
| chr2:54974113
|
A | T | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3431-246T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974113 | ||||||
| chr2:54974225
|
G | C | 8 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(5): Show | 8 | HG02647.hp2 HG02896.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3431-358C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974225 | ||||||
| chr2:54974285
|
C | T | 5 | a0002c0002t0001g0049a0002c0002t0003g0050a0002c0002t0003g0051others(2): Show | 5 | HG01070.hp1 HG02683.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.3430+410G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974285 | ||||||
| chr2:54974340
|
C | G | 1 | a0001c0001t0006g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3430+355G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974340 | ||||||
| chr2:54974560
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3430+135G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974560 | ||||||
| chr2:54974592
|
C | T | 1 | a0001c0001t0013g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3430+103G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974592 | ||||||
| chr2:54974863
|
G | C | 1 | a0005c0004t0002g0167 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3361-99C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54974863 | ||||||
| chr2:54974863
|
G | T | 2 | a0001c0001t0003g0130a0001c0001t0003g0131 | 2 | NA18954.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.3361-99C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54974863 | ||||||
| chr2:54975120
|
T | G | 1 | a0002c0002t0003g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3361-356A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975120 | ||||||
| chr2:54975319
|
G | A | 57 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(54): Show | 60 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.3361-555C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975319 | ||||||
| chr2:54975343
|
C | G | 1 | a0001c0008t0008g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3361-579G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975343 | ||||||
| chr2:54975369
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3361-605A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975369 | ||||||
| chr2:54975401
|
C | G | 1 | a0001c0008t0008g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3361-637G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975401 | ||||||
| chr2:54975503
|
T | C | 3 | a0003c0003t0004g0004a0003c0003t0014g0071a0003c0003t0014g0072 | 4 | HG01891.hp2 HG03209.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3361-739A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975503 | ||||||
| chr2:54975513
|
C | T | 248 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(245): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.3361-749G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975513 | ||||||
| chr2:54975624
|
A | G | 4 | a0001c0001t0002g0175a0001c0001t0002g0292a0001c0010t0002g0320others(1): Show | 4 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.3361-860T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975624 | ||||||
| chr2:54975773
|
T | C | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3361-1009A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975773 | ||||||
| chr2:54975792
|
T | G | 1 | a0002c0002t0003g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3361-1028A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975792 | ||||||
| chr2:54975915
|
T | A | 2 | a0001c0001t0001g0074a0002c0002t0003g0031 | 2 | HG00544.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3361-1151A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975915 | ||||||
| chr2:54975947
|
T | A | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-1183A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975947 | ||||||
| chr2:54975948
|
A | T | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-1184T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975948 | ||||||
| chr2:54975949
|
T | A | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-1185A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975949 | ||||||
| chr2:54976071
|
A | G | 9 | a0004c0005t0001g0323a0004c0005t0001g0324a0004c0005t0001g0325others(6): Show | 9 | HG02109.hp1 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.3361-1307T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976071 | ||||||
| chr2:54976192
|
G | C | 8 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0237others(5): Show | 8 | HG02080.hp1 NA18947.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.3361-1428C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976192 | ||||||
| chr2:54976231
|
T | A | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-1467A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976231 | ||||||
| chr2:54976259
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3361-1495C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976259 | ||||||
| chr2:54976316
|
C | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3361-1552G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976316 | ||||||
| chr2:54976512
|
G | A | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.3361-1748C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976512 | ||||||
| chr2:54976587
|
G | A | 1 | a0005c0004t0002g0169 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3361-1823C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976587 | ||||||
| chr2:54976604
|
A | C | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3361-1840T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976604 | ||||||
| chr2:54976795
|
C | G | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(89): Show | 101 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.3361-2031G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976795 | ||||||
| chr2:54976838
|
C | G | 1 | a0001c0001t0006g0304 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3361-2074G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976838 | ||||||
| chr2:54976892
|
A | C | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(89): Show | 101 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.3361-2128T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976892 | ||||||
| chr2:54976907
|
A | G | 4 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0006g0309others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.3361-2143T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976907 | ||||||
| chr2:54976947
|
G | T | 1 | a0001c0001t0002g0189 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3361-2183C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976947 | ||||||
| chr2:54977017
|
G | A | 1 | a0005c0004t0002g0167 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3361-2253C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977017 | ||||||
| chr2:54977029
|
C | T | 58 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(55): Show | 59 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.3361-2265G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977029 | ||||||
| chr2:54977083
|
G | A | 4 | a0006c0006t0002g0003a0006c0006t0002g0301a0006c0006t0002g0302others(1): Show | 6 | HG00738.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3361-2319C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977083 | ||||||
| chr2:54977127
|
TA | T | 12 | a0001c0001t0005g0011a0001c0001t0005g0281a0001c0001t0005g0282others(9): Show | 13 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.3361-2364delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977127 | ||||||
| chr2:54977170
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3361-2406G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977170 | ||||||
| chr2:54977362
|
G | C | 183 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3361-2598C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977362 | ||||||
| chr2:54977374
|
C | A | 1 | a0001c0001t0001g0248 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3361-2610G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977374 | ||||||
| chr2:54977401
|
A | G | 10 | a0001c0001t0001g0214a0001c0001t0007g0332a0001c0001t0007g0333others(7): Show | 10 | HG02280.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3361-2637T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977401 | ||||||
| chr2:54977406
|
G | GT | 178 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(175): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.3361-2643dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977406 | ||||||
| chr2:54977406
|
G | GTT | 20 | a0001c0001t0001g0087a0001c0001t0001g0214a0001c0001t0002g0207others(17): Show | 20 | HG02132.hp2 HG02145.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.3361-2644_3361-264 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977406 | ||||||
| chr2:54977439
|
T | G | 1 | a0001c0001t0001g0314 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3361-2675A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977439 | ||||||
| chr2:54977469
|
C | T | 7 | a0001c0001t0002g0008a0001c0001t0002g0141a0001c0001t0002g0155others(4): Show | 8 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.3361-2705G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977469 | ||||||
| chr2:54977631
|
T | A | 1 | a0001c0001t0002g0133 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3361-2867A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977631 | ||||||
| chr2:54977660
|
A | T | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-2896T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977660 | ||||||
| chr2:54977664
|
C | G | 298 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(295): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.3361-2900G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977664 | ||||||
| chr2:54977685
|
G | A | 1 | a0001c0008t0008g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3361-2921C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977685 | ||||||
| chr2:54977729
|
T | C | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3361-2965A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977729 | ||||||
| chr2:54977759
|
G | T | 4 | a0001c0001t0002g0081a0001c0001t0002g0133a0001c0001t0002g0157others(1): Show | 4 | NA18965.hp1 NA19056.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.3361-2995C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977759 | ||||||
| chr2:54977895
|
G | A | 1 | a0001c0001t0002g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3361-3131C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977895 | ||||||
| chr2:54977951
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3361-3187T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977951 | ||||||
| chr2:54977956
|
T | C | 298 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(295): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.3361-3192A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977956 | ||||||
| chr2:54977988
|
T | C | 182 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(179): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.3361-3224A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977988 | ||||||
| chr2:54978054
|
T | G | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3361-3290A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978054 | ||||||
| chr2:54978111
|
A | C | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201 | 3 | HG03041.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3361-3347T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978111 | ||||||
| chr2:54978126
|
C | A | 298 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(295): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.3361-3362G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978126 | ||||||
| chr2:54978187
|
T | C | 9 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(6): Show | 9 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3361-3423A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978187 | ||||||
| chr2:54978335
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3361-3571G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978335 | ||||||
| chr2:54978386
|
G | A | 2 | a0001c0001t0002g0172a0001c0001t0002g0312 | 2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.3361-3622C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978386 | ||||||
| chr2:54978390
|
C | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0127 | 3 | HG02559.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3361-3626G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978390 | ||||||
| chr2:54978393
|
C | T | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3361-3629G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978393 | ||||||
| chr2:54978405
|
T | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | NA18947.hp2 NA18967.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.3361-3641A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978405 | ||||||
| chr2:54978417
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3361-3653G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978417 | ||||||
| chr2:54978431
|
C | CA | 94 | a0001c0001t0001g0100a0001c0001t0001g0124a0001c0001t0001g0216others(91): Show | 103 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.3361-3668dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978431 | ||||||
| chr2:54978431
|
C | CAA | 15 | a0001c0001t0002g0132a0001c0001t0002g0134a0001c0001t0002g0142others(12): Show | 15 | HG00323.hp1 HG00609.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.3361-3669_3361-366 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978431 | ||||||
| chr2:54978431
|
CA | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(79): Show | 85 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.3361-3668delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978431 | ||||||
| chr2:54978431
|
CAA | C | 10 | a0001c0001t0001g0214a0001c0001t0007g0332a0001c0001t0007g0333others(7): Show | 10 | HG02280.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3361-3669_3361-366 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978431 | ||||||
| chr2:54978811
|
A | G | 250 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(247): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.3360+3704T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978811 | ||||||
| chr2:54978869
|
C | T | 9 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(6): Show | 9 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3360+3646G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978869 | ||||||
| chr2:54978923
|
G | A | 13 | a0001c0001t0001g0214a0001c0001t0007g0332a0001c0001t0007g0333others(10): Show | 13 | HG02145.hp1 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.3360+3592C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978923 | ||||||
| chr2:54978938
|
A | T | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3360+3577T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978938 | ||||||
| chr2:54978998
|
A | C | 1 | a0001c0001t0005g0296 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3360+3517T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978998 | ||||||
| chr2:54979011
|
T | A | 2 | a0001c0001t0007g0332a0001c0001t0007g0335 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3360+3504A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979011 | ||||||
| chr2:54979052
|
A | AT | 15 | a0001c0001t0001g0121a0001c0001t0001g0252a0001c0001t0002g0158others(12): Show | 15 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.3360+3462dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979052 | ||||||
| chr2:54979052
|
AT | A | 9 | a0001c0001t0002g0144a0001c0001t0002g0189a0001c0001t0002g0209others(6): Show | 12 | HG00423.hp2 HG00738.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.3360+3462delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979052 | ||||||
| chr2:54979170
|
A | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3360+3345T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979170 | ||||||
| chr2:54979193
|
C | A | 1 | a0002c0002t0003g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3360+3322G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979193 | ||||||
| chr2:54979208
|
A | T | 11 | a0001c0001t0002g0008a0001c0001t0002g0134a0001c0001t0002g0141others(8): Show | 12 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.3360+3307T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979208 | ||||||
| chr2:54979227
|
GT | G | 178 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(175): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.3360+3287delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979227 | ||||||
| chr2:54979227
|
GTT | G | 9 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(6): Show | 9 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3360+3286_3360+328 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979227 | ||||||
| chr2:54979393
|
T | G | 1 | a0001c0001t0004g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3360+3122A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979393 | ||||||
| chr2:54979463
|
G | A | 2 | a0001c0008t0018g0067a0015c0020t0002g0315 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3360+3052C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979463 | ||||||
| chr2:54979547
|
T | C | 2 | a0005c0004t0002g0170a0005c0004t0002g0191 | 2 | HG02523.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.3360+2968A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979547 | ||||||
| chr2:54979642
|
G | A | 4 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0023t0001g0322others(1): Show | 4 | HG02040.hp2 HG02165.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.3360+2873C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979642 | ||||||
| chr2:54979927
|
C | T | 15 | a0001c0001t0001g0214a0001c0001t0007g0332a0001c0001t0007g0333others(12): Show | 15 | HG02145.hp1 HG02280.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.3360+2588G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979927 | ||||||
| chr2:54980017
|
A | T | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3360+2498T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980017 | ||||||
| chr2:54980074
|
T | A | 2 | a0004c0005t0001g0325a0004c0005t0001g0327 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3360+2441A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980074 | ||||||
| chr2:54980116
|
T | C | 1 | a0005c0004t0002g0167 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3360+2399A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980116 | ||||||
| chr2:54980266
|
C | T | 1 | a0001c0001t0024g0154 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3360+2249G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980266 | ||||||
| chr2:54980485
|
A | T | 2 | a0001c0008t0018g0067a0015c0020t0002g0315 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3360+2030T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980485 | ||||||
| chr2:54980545
|
T | A | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3360+1970A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980545 | ||||||
| chr2:54980557
|
C | T | 58 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(55): Show | 59 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.3360+1958G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980557 | ||||||
| chr2:54980583
|
T | G | 1 | a0001c0001t0005g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3360+1932A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980583 | ||||||
| chr2:54980759
|
C | T | 249 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(246): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.3360+1756G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980759 | ||||||
| chr2:54980934
|
T | C | 4 | a0002c0002t0003g0027a0002c0002t0003g0028a0002c0002t0003g0029others(1): Show | 4 | NA18952.hp1 NA18960.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.3360+1581A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980934 | ||||||
| chr2:54980992
|
A | G | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3360+1523T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980992 | ||||||
| chr2:54981190
|
G | A | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3360+1325C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981190 | ||||||
| chr2:54981229
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3360+1286T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981229 | ||||||
| chr2:54981276
|
TG | T | 3 | a0001c0001t0002g0292a0001c0010t0002g0320a0001c0010t0002g0321 | 3 | HG01109.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3360+1238delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981276 | ||||||
| chr2:54981277
|
G | GT | 9 | a0001c0001t0002g0186a0001c0001t0002g0189a0001c0001t0002g0204others(6): Show | 9 | HG01952.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3360+1237dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981277 | ||||||
| chr2:54981278
|
T | G | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3360+1237A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981278 | ||||||
| chr2:54981282
|
TG | T | 13 | a0001c0001t0001g0214a0001c0001t0001g0266a0001c0001t0002g0159others(10): Show | 13 | HG00099.hp2 HG00423.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3360+1232delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981282 | ||||||
| chr2:54981283
|
G | T | 192 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(189): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.3360+1232C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981283 | ||||||
| chr2:54981283
|
GT | G | 7 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(4): Show | 7 | HG02647.hp2 HG02896.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3360+1231delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981283 | ||||||
| chr2:54981284
|
T | G | 1 | a0001c0001t0002g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3360+1231A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981284 | ||||||
| chr2:54981295
|
T | A | 1 | a0001c0001t0005g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3360+1220A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981295 | ||||||
| chr2:54981296
|
A | T | 3 | a0001c0001t0001g0216a0014c0018t0020g0164a0016c0016t0001g0107 | 3 | NA18906.hp1 NA18985.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3360+1219T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981296 | ||||||
| chr2:54981338
|
A | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0248 | 2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3360+1177T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981338 | ||||||
| chr2:54981664
|
G | C | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3360+851C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981664 | ||||||
| chr2:54981732
|
G | A | 249 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(246): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.3360+783C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981732 | ||||||
| chr2:54981733
|
T | C | 13 | a0001c0001t0001g0214a0001c0001t0007g0332a0001c0001t0007g0333others(10): Show | 13 | HG02145.hp1 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.3360+782A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981733 | ||||||
| chr2:54981817
|
A | ATATGAAT others(19): Show |
152 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(149): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.3360+697_3360+698i others(28): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981817 | ||||||
| chr2:54981873
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3360+642G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981873 | ||||||
| chr2:54981901
|
GATTA | G | 3 | a0001c0001t0006g0303a0001c0001t0006g0309a0001c0001t0006g0310 | 3 | HG02145.hp2 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3360+610_3360+613d others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981901 | ||||||
| chr2:54981947
|
C | CTA | 13 | a0001c0001t0001g0214a0001c0001t0007g0332a0001c0001t0007g0333others(10): Show | 13 | HG02145.hp1 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.3360+566_3360+567d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981947 | ||||||
| chr2:54982041
|
G | A | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(84): Show | 96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.3360+474C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982041 | ||||||
| chr2:54982048
|
G | A | 1 | a0002c0002t0003g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3360+467C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982048 | ||||||
| chr2:54982090
|
G | A | 28 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0139others(25): Show | 30 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.3360+425C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982090 | ||||||
| chr2:54982099
|
G | A | 3 | a0001c0001t0010g0273a0001c0001t0010g0275a0001c0001t0010g0276 | 3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3360+416C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982099 | ||||||
| chr2:54982143
|
ACGGGGTT others(1): Show |
A | 30 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(27): Show | 31 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.3360+364_3360+371d others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982143 | ||||||
| chr2:54982252
|
G | A | 1 | a0002c0002t0003g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3360+263C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982252 | ||||||
| chr2:54982850
|
A | G | 2 | a0001c0001t0004g0198a0001c0001t0004g0218 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3222-197T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54982850 | ||||||
| chr2:54982888
|
A | T | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3222-235T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54982888 | ||||||
| chr2:54982970
|
T | C | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3222-317A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54982970 | ||||||
| chr2:54982979
|
G | T | 1 | a0002c0002t0003g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3222-326C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54982979 | ||||||
| chr2:54983065
|
G | GT | 6 | a0001c0001t0002g0204a0001c0001t0005g0277a0002c0002t0003g0027others(3): Show | 6 | NA18952.hp1 NA18960.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.3222-413dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983065 | ||||||
| chr2:54983135
|
T | C | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3222-482A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983135 | ||||||
| chr2:54983207
|
G | A | 1 | a0001c0001t0002g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3222-554C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983207 | ||||||
| chr2:54983280
|
C | T | 4 | a0004c0005t0001g0324a0004c0005t0001g0326a0004c0005t0001g0328others(1): Show | 4 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3222-627G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983280 | ||||||
| chr2:54983321
|
T | TAATA | 77 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0134others(74): Show | 78 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.3222-672_3222-669d others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | ||||||
| chr2:54983321
|
T | TAATAAAT others(1): Show |
9 | a0001c0001t0005g0296a0001c0001t0005g0299a0001c0001t0005g0300others(6): Show | 9 | HG01168.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3222-676_3222-669d others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | ||||||
| chr2:54983321
|
T | TAATAAAT others(5): Show |
5 | a0001c0001t0003g0129a0001c0001t0005g0294a0001c0001t0005g0297others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3222-680_3222-669d others(14): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | ||||||
| chr2:54983321
|
TAATA | T | 79 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(76): Show | 80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3222-672_3222-669d others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | ||||||
| chr2:54983321
|
TAATAAAT others(1): Show |
T | 8 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(5): Show | 8 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3222-676_3222-669d others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | ||||||
| chr2:54983352
|
T | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(32): Show | 36 | HG00735.hp2 HG01928.hp2 HG02080.hp1 others(33): Show |
intron_variant | MODIFIER | c.3222-699A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983352 | ||||||
| chr2:54983368
|
G | A | 1 | a0013c0019t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3222-715C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983368 | ||||||
| chr2:54983469
|
T | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(79): Show | 83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3222-816A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983469 | ||||||
| chr2:54983518
|
A | C | 1 | a0001c0001t0005g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3222-865T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983518 | ||||||
| chr2:54983582
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3222-929G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983582 | ||||||
| chr2:54983617
|
T | A | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3222-964A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983617 | ||||||
| chr2:54983658
|
G | A | 2 | a0001c0001t0012g0268a0015c0020t0002g0315 | 2 | HG03516.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3222-1005C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983658 | ||||||
| chr2:54983720
|
C | T | 247 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(244): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3222-1067G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983720 | ||||||
| chr2:54983721
|
G | A | 1 | a0002c0002t0003g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3222-1068C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983721 | ||||||
| chr2:54984010
|
T | G | 8 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(5): Show | 8 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3222-1357A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984010 | ||||||
| chr2:54984036
|
C | A | 1 | a0001c0001t0006g0304 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3222-1383G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984036 | ||||||
| chr2:54984160
|
C | A | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3222-1507G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984160 | ||||||
| chr2:54984179
|
C | G | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3222-1526G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984179 | ||||||
| chr2:54984188
|
C | A | 247 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(244): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3222-1535G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984188 | ||||||
| chr2:54984310
|
G | A | 247 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(244): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3222-1657C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984310 | ||||||
| chr2:54984394
|
A | T | 1 | a0001c0001t0009g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3222-1741T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984394 | ||||||
| chr2:54984397
|
T | C | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3222-1744A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984397 | ||||||
| chr2:54984501
|
G | T | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3222-1848C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984501 | ||||||
| chr2:54984709
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3222-2056A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984709 | ||||||
| chr2:54984748
|
C | G | 7 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(4): Show | 7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3222-2095G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984748 | ||||||
| chr2:54984806
|
A | G | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3222-2153T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984806 | ||||||
| chr2:54984807
|
G | A | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3222-2154C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984807 | ||||||
| chr2:54984884
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3222-2231A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984884 | ||||||
| chr2:54985043
|
G | T | 247 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(244): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3222-2390C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985043 | ||||||
| chr2:54985048
|
A | G | 2 | a0002c0002t0002g0047a0002c0002t0002g0060 | 2 | NA18978.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.3222-2395T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985048 | ||||||
| chr2:54985153
|
C | CT | 58 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(55): Show | 59 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.3221+2337dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | ||||||
| chr2:54985153
|
C | CTT | 65 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(62): Show | 65 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3221+2336_3221+233 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | ||||||
| chr2:54985153
|
C | CTTT | 23 | a0001c0001t0001g0078a0001c0001t0001g0093a0001c0001t0001g0100others(20): Show | 23 | HG01175.hp2 HG01361.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.3221+2335_3221+233 others(7): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | ||||||
| chr2:54985153
|
C | CTTTT | 11 | a0001c0001t0001g0089a0001c0001t0001g0094a0001c0001t0001g0095others(8): Show | 11 | HG00099.hp1 HG01256.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.3221+2334_3221+233 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | ||||||
| chr2:54985153
|
C | CTTTTTTT others(6): Show |
1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3221+2325_3221+233 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | ||||||
| chr2:54985153
|
CT | C | 77 | a0001c0001t0001g0214a0001c0001t0001g0250a0001c0001t0002g0001others(74): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.3221+2337delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | ||||||
| chr2:54985153
|
CTT | C | 30 | a0001c0001t0002g0136a0001c0001t0005g0277a0001c0001t0005g0278others(27): Show | 30 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.3221+2336_3221+233 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | ||||||
| chr2:54985153
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0003g0036 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3221+2325_3221+233 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | ||||||
| chr2:54985153
|
CTTTTTTT others(9): Show |
C | 6 | a0001c0001t0001g0010a0001c0001t0001g0227a0001c0001t0001g0228others(3): Show | 7 | NA18951.hp1 NA18971.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.3221+2322_3221+233 others(20): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | ||||||
| chr2:54985191
|
G | A | 3 | a0001c0001t0010g0273a0001c0001t0010g0275a0001c0001t0010g0276 | 3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3221+2300C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985191 | ||||||
| chr2:54985201
|
T | C | 240 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(237): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3221+2290A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985201 | ||||||
| chr2:54985202
|
T | C | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3221+2289A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985202 | ||||||
| chr2:54985288
|
T | C | 1 | a0001c0001t0004g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3221+2203A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985288 | ||||||
| chr2:54985339
|
T | G | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3221+2152A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985339 | ||||||
| chr2:54985359
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(78): Show | 82 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.3221+2132A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985359 | ||||||
| chr2:54985437
|
G | C | 7 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(4): Show | 7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3221+2054C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985437 | ||||||
| chr2:54985454
|
T | C | 247 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(244): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3221+2037A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985454 | ||||||
| chr2:54985769
|
A | C | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+1722T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985769 | ||||||
| chr2:54985787
|
G | T | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+1704C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985787 | ||||||
| chr2:54985789
|
T | C | 122 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.3221+1702A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985789 | ||||||
| chr2:54986174
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3221+1317T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986174 | ||||||
| chr2:54986184
|
G | A | 30 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(27): Show | 32 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.3221+1307C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986184 | ||||||
| chr2:54986262
|
G | A | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+1229C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986262 | ||||||
| chr2:54986263
|
A | G | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+1228T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986263 | ||||||
| chr2:54986297
|
T | C | 1 | a0002c0002t0001g0056 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3221+1194A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986297 | ||||||
| chr2:54986727
|
C | T | 1 | a0001c0001t0013g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3221+764G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986727 | ||||||
| chr2:54986728
|
G | A | 3 | a0001c0001t0002g0135a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG01074.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3221+763C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986728 | ||||||
| chr2:54986733
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3221+758A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986733 | ||||||
| chr2:54986776
|
C | T | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3221+715G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986776 | ||||||
| chr2:54986785
|
T | C | 7 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0012g0264others(4): Show | 7 | HG02040.hp2 HG02132.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3221+706A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986785 | ||||||
| chr2:54986854
|
C | CAATTAAA others(7): Show |
1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+623_3221+636d others(16): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986854 | ||||||
| chr2:54986863
|
A | G | 2 | a0001c0008t0018g0067a0015c0020t0002g0315 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3221+628T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986863 | ||||||
| chr2:54986879
|
C | T | 247 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(244): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3221+612G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986879 | ||||||
| chr2:54986929
|
T | C | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3221+562A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986929 | ||||||
| chr2:54987309
|
C | A | 1 | a0001c0001t0001g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3221+182G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54987309 | ||||||
| chr2:54987482
|
A | C | 185 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(182): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.3221+9T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54987482 | ||||||
| chr2:54987776
|
C | G | 247 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(244): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3014-78G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987776 | ||||||
| chr2:54987842
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3014-144A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987842 | ||||||
| chr2:54987878
|
T | A | 1 | a0001c0001t0002g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3014-180A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987878 | ||||||
| chr2:54987967
|
G | A | 1 | a0001c0001t0005g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3014-269C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987967 | ||||||
| chr2:54987999
|
A | T | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3014-301T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987999 | ||||||
| chr2:54988332
|
G | T | 1 | a0001c0001t0005g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3014-634C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988332 | ||||||
| chr2:54988347
|
A | C | 6 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261others(3): Show | 6 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3014-649T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988347 | ||||||
| chr2:54988481
|
G | A | 29 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(26): Show | 31 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.3014-783C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988481 | ||||||
| chr2:54988502
|
T | C | 1 | a0001c0001t0013g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3014-804A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988502 | ||||||
| chr2:54988689
|
G | A | 247 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(244): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3014-991C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988689 | ||||||
| chr2:54988954
|
C | T | 7 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(4): Show | 7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3014-1256G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988954 | ||||||
| chr2:54988982
|
T | C | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-1284A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988982 | ||||||
| chr2:54988991
|
T | C | 32 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(29): Show | 34 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.3014-1293A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988991 | ||||||
| chr2:54989084
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3014-1386A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989084 | ||||||
| chr2:54989085
|
G | A | 8 | a0001c0001t0001g0214a0001c0001t0007g0332a0001c0001t0007g0333others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3014-1387C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989085 | ||||||
| chr2:54989337
|
C | T | 1 | a0001c0001t0005g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3014-1639G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989337 | ||||||
| chr2:54989372
|
C | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-1674G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989372 | ||||||
| chr2:54989409
|
C | A | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(85): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3014-1711G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989409 | ||||||
| chr2:54989417
|
G | A | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3014-1719C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989417 | ||||||
| chr2:54989517
|
G | A | 2 | a0001c0001t0015g0145a0001c0001t0015g0254 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3014-1819C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989517 | ||||||
| chr2:54989771
|
G | T | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3014-2073C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989771 | ||||||
| chr2:54989857
|
A | T | 3 | a0001c0001t0010g0273a0001c0001t0010g0275a0001c0001t0010g0276 | 3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3014-2159T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989857 | ||||||
| chr2:54989998
|
C | T | 7 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(4): Show | 7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3014-2300G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989998 | ||||||
| chr2:54990182
|
T | C | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3014-2484A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990182 | ||||||
| chr2:54990294
|
A | T | 32 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(29): Show | 34 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.3014-2596T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990294 | ||||||
| chr2:54990310
|
C | CG | 3 | a0001c0001t0001g0113a0001c0001t0010g0276a0014c0018t0020g0164 | 3 | HG02145.hp1 NA18956.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3014-2613dupC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990310 | ||||||
| chr2:54990324
|
G | C | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-2626C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990324 | ||||||
| chr2:54990382
|
T | C | 51 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0003g0128others(48): Show | 51 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3014-2684A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990382 | ||||||
| chr2:54990443
|
G | C | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3014-2745C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990443 | ||||||
| chr2:54990468
|
T | C | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-2770A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990468 | ||||||
| chr2:54990478
|
TTAA | T | 3 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261 | 3 | HG02818.hp2 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3014-2783_3014-278 others(7): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990478 | ||||||
| chr2:54990651
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3014-2953A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990651 | ||||||
| chr2:54990681
|
T | C | 1 | a0017c0015t0008g0308 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3014-2983A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990681 | ||||||
| chr2:54990721
|
T | A | 1 | a0011c0022t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3014-3023A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990721 | ||||||
| chr2:54990722
|
A | T | 1 | a0011c0022t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3014-3024T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990722 | ||||||
| chr2:54990787
|
T | A | 1 | a0001c0001t0001g0256 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3014-3089A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990787 | ||||||
| chr2:54990816
|
C | T | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3014-3118G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990816 | ||||||
| chr2:54990835
|
G | A | 51 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0003g0128others(48): Show | 51 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3014-3137C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990835 | ||||||
| chr2:54990871
|
C | T | 2 | a0001c0001t0009g0149a0001c0001t0009g0316 | 2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3014-3173G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990871 | ||||||
| chr2:54990890
|
A | T | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(84): Show | 96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.3014-3192T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990890 | ||||||
| chr2:54990990
|
G | A | 1 | a0005c0004t0002g0167 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3014-3292C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990990 | ||||||
| chr2:54991382
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3014-3684A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991382 | ||||||
| chr2:54991622
|
C | T | 1 | a0001c0008t0008g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3014-3924G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991622 | ||||||
| chr2:54991655
|
G | A | 82 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(79): Show | 83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3014-3957C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991655 | ||||||
| chr2:54991669
|
G | T | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(86): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.3014-3971C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991669 | ||||||
| chr2:54991722
|
G | C | 1 | a0002c0002t0019g0023 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3014-4024C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991722 | ||||||
| chr2:54991864
|
A | T | 2 | a0003c0003t0014g0071a0003c0003t0014g0072 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3014-4166T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991864 | ||||||
| chr2:54991969
|
C | A | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3014-4271G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991969 | ||||||
| chr2:54991999
|
C | T | 31 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(28): Show | 32 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.3014-4301G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991999 | ||||||
| chr2:54992199
|
A | C | 1 | a0001c0001t0002g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3014-4501T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992199 | ||||||
| chr2:54992380
|
G | T | 34 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(31): Show | 35 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.3014-4682C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992380 | ||||||
| chr2:54992493
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3014-4795T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992493 | ||||||
| chr2:54992523
|
C | T | 2 | a0001c0001t0005g0287a0001c0001t0005g0288 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3014-4825G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992523 | ||||||
| chr2:54992663
|
G | A | 34 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(31): Show | 35 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.3014-4965C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992663 | ||||||
| chr2:54992674
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3014-4976T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992674 | ||||||
| chr2:54992760
|
A | C | 1 | a0001c0001t0021g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3014-5062T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992760 | ||||||
| chr2:54992853
|
A | C | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(84): Show | 96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.3014-5155T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992853 | ||||||
| chr2:54992885
|
C | T | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(84): Show | 96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.3014-5187G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992885 | ||||||
| chr2:54992896
|
C | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-5198G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992896 | ||||||
| chr2:54993028
|
T | G | 3 | a0001c0001t0010g0273a0001c0001t0010g0275a0001c0001t0010g0276 | 3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3014-5330A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993028 | ||||||
| chr2:54993061
|
G | A | 150 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(147): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.3014-5363C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993061 | ||||||
| chr2:54993073
|
CG | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(71): Show | 75 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.3014-5376delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993073 | ||||||
| chr2:54993074
|
G | GA | 29 | a0001c0001t0004g0193a0001c0001t0005g0011a0001c0001t0005g0278others(26): Show | 30 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.3014-5377_3014-537 others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993074 | ||||||
| chr2:54993074
|
G | GAA | 3 | a0001c0001t0004g0194a0001c0001t0005g0293a0001c0001t0005g0298 | 3 | HG02109.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3014-5377_3014-537 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993074 | ||||||
| chr2:54993074
|
GGA | G | 32 | a0001c0001t0001g0112a0001c0001t0001g0214a0001c0001t0004g0077others(29): Show | 34 | HG01109.hp1 HG01346.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.3014-5378_3014-537 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993074 | ||||||
| chr2:54993075
|
G | A | 37 | a0001c0001t0001g0118a0001c0001t0004g0193a0001c0001t0004g0194others(34): Show | 38 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.3014-5377C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993075 | ||||||
| chr2:54993075
|
G | GA | 6 | a0001c0001t0001g0240a0001c0001t0002g0187a0001c0001t0002g0311others(3): Show | 6 | HG01175.hp2 HG01361.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-5378dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993075 | ||||||
| chr2:54993075
|
GA | G | 12 | a0001c0001t0001g0236a0001c0001t0002g0132a0001c0008t0018g0067others(9): Show | 12 | HG00323.hp1 HG02109.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.3014-5378delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993075 | ||||||
| chr2:54993076
|
A | G | 1 | a0001c0001t0002g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3014-5378T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993076 | ||||||
| chr2:54993099
|
G | C | 1 | a0001c0001t0012g0268 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3014-5401C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993099 | ||||||
| chr2:54993122
|
G | A | 1 | a0001c0001t0002g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3014-5424C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993122 | ||||||
| chr2:54993170
|
A | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-5472T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993170 | ||||||
| chr2:54993224
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3014-5526A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993224 | ||||||
| chr2:54993381
|
T | A | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3014-5683A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993381 | ||||||
| chr2:54993439
|
G | C | 1 | a0010c0024t0006g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3014-5741C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993439 | ||||||
| chr2:54993448
|
C | T | 79 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(76): Show | 80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3014-5750G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993448 | ||||||
| chr2:54993671
|
T | C | 1 | a0001c0001t0010g0273 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3014-5973A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993671 | ||||||
| chr2:54993824
|
T | C | 174 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(171): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.3014-6126A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993824 | ||||||
| chr2:54994013
|
A | G | 1 | a0001c0001t0004g0194 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3014-6315T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994013 | ||||||
| chr2:54994147
|
T | C | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-6449A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994147 | ||||||
| chr2:54994371
|
A | G | 1 | a0001c0008t0008g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3014-6673T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994371 | ||||||
| chr2:54994410
|
C | T | 26 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(23): Show | 28 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.3014-6712G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994410 | ||||||
| chr2:54994591
|
A | G | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-6893T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994591 | ||||||
| chr2:54994611
|
G | C | 1 | a0001c0001t0005g0299 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3014-6913C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994611 | ||||||
| chr2:54994699
|
G | T | 39 | a0001c0001t0004g0138a0001c0001t0004g0197a0001c0001t0004g0202others(36): Show | 40 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.3014-7001C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994699 | ||||||
| chr2:54994861
|
A | G | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-7163T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994861 | ||||||
| chr2:54994944
|
T | C | 2 | a0001c0001t0007g0332a0001c0001t0007g0335 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3014-7246A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994944 | ||||||
| chr2:54994966
|
C | T | 1 | a0001c0001t0004g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3014-7268G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994966 | ||||||
| chr2:54994970
|
C | T | 153 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(150): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.3014-7272G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994970 | ||||||
| chr2:54994996
|
G | A | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(85): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3014-7298C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994996 | ||||||
| chr2:54995029
|
G | C | 1 | a0001c0001t0004g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3014-7331C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995029 | ||||||
| chr2:54995082
|
A | G | 3 | a0001c0001t0010g0273a0001c0001t0010g0275a0001c0001t0010g0276 | 3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3014-7384T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995082 | ||||||
| chr2:54995109
|
C | A | 2 | a0001c0001t0005g0293a0001c0001t0005g0298 | 2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3014-7411G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995109 | ||||||
| chr2:54995202
|
T | C | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-7504A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995202 | ||||||
| chr2:54995256
|
T | A | 1 | a0001c0001t0005g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3014-7558A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995256 | ||||||
| chr2:54995289
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3014-7591T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995289 | ||||||
| chr2:54995494
|
A | C | 80 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(77): Show | 81 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3014-7796T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995494 | ||||||
| chr2:54995544
|
G | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(77): Show | 81 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3014-7846C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995544 | ||||||
| chr2:54995569
|
A | G | 1 | a0005c0004t0002g0167 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3014-7871T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995569 | ||||||
| chr2:54995688
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3014-7990G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995688 | ||||||
| chr2:54995881
|
T | G | 1 | a0007c0007t0013g0065 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3014-8183A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995881 | ||||||
| chr2:54995971
|
T | A | 51 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0003g0128others(48): Show | 51 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3014-8273A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995971 | ||||||
| chr2:54995988
|
G | C | 1 | a0001c0001t0012g0268 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3014-8290C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995988 | ||||||
| chr2:54996009
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3014-8311C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996009 | ||||||
| chr2:54996043
|
T | C | 1 | a0001c0001t0006g0304 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3014-8345A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996043 | ||||||
| chr2:54996146
|
C | T | 148 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(145): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.3014-8448G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996146 | ||||||
| chr2:54996223
|
A | G | 1 | a0002c0002t0003g0038 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3014-8525T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996223 | ||||||
| chr2:54996286
|
C | T | 10 | a0001c0001t0025g0080a0004c0005t0001g0323a0004c0005t0001g0324others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3014-8588G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996286 | ||||||
| chr2:54996319
|
G | A | 24 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(21): Show | 26 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.3014-8621C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996319 | ||||||
| chr2:54996502
|
G | A | 56 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(53): Show | 57 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.3014-8804C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996502 | ||||||
| chr2:54996550
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3014-8852C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996550 | ||||||
| chr2:54996698
|
C | T | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-9000G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996698 | ||||||
| chr2:54997037
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3014-9339G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997037 | ||||||
| chr2:54997273
|
C | T | 6 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-9575G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997273 | ||||||
| chr2:54997278
|
T | C | 1 | a0001c0001t0002g0157 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3014-9580A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997278 | ||||||
| chr2:54997321
|
C | T | 6 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-9623G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997321 | ||||||
| chr2:54997357
|
A | G | 1 | a0017c0015t0008g0308 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3014-9659T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997357 | ||||||
| chr2:54997357
|
A | T | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3014-9659T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997357 | ||||||
| chr2:54997522
|
T | C | 6 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-9824A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997522 | ||||||
| chr2:54997532
|
A | C | 19 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(16): Show | 19 | HG02080.hp1 NA18942.hp2 NA18947.hp2 others(16): Show |
intron_variant | MODIFIER | c.3014-9834T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997532 | ||||||
| chr2:54997567
|
T | C | 11 | a0001c0001t0001g0214a0001c0001t0007g0332a0001c0001t0007g0333others(8): Show | 11 | HG02109.hp1 HG02280.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3014-9869A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997567 | ||||||
| chr2:54997574
|
T | C | 6 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-9876A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997574 | ||||||
| chr2:54997775
|
T | C | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-10077A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997775 | ||||||
| chr2:54998061
|
G | A | 1 | a0002c0002t0003g0037 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3014-10363C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998061 | ||||||
| chr2:54998064
|
A | C | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3014-10366T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998064 | ||||||
| chr2:54998167
|
T | C | 76 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(73): Show | 77 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.3014-10469A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998167 | ||||||
| chr2:54998246
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3014-10548C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998246 | ||||||
| chr2:54998330
|
TA | T | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0013g0064others(2): Show | 5 | HG01167.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3014-10633delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998330 | ||||||
| chr2:54998494
|
T | C | 1 | a0001c0001t0013g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3014-10796A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998494 | ||||||
| chr2:54998666
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3014-10968A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998666 | ||||||
| chr2:54998683
|
C | G | 1 | a0001c0001t0005g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3014-10985G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998683 | ||||||
| chr2:54998701
|
G | A | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3014-11003C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998701 | ||||||
| chr2:54998809
|
T | C | 1 | a0001c0001t0013g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3014-11111A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998809 | ||||||
| chr2:54998873
|
G | A | 218 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.3014-11175C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998873 | ||||||
| chr2:54999403
|
T | C | 3 | a0004c0005t0001g0323a0004c0005t0001g0325a0004c0005t0001g0327 | 3 | HG02109.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3014-11705A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54999403 | ||||||
| chr2:54999792
|
C | T | 1 | a0001c0001t0005g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3014-12094G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54999792 | ||||||
| chr2:54999809
|
G | A | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-12111C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54999809 | ||||||
| chr2:54999891
|
T | C | 10 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(7): Show | 10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3014-12193A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54999891 | ||||||
| chr2:55000054
|
T | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0182 | 2 | HG02165.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.3014-12356A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000054 | ||||||
| chr2:55000095
|
C | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(141): Show | 148 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.3014-12397G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000095 | ||||||
| chr2:55000113
|
A | G | 1 | a0001c0001t0015g0254 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3014-12415T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000113 | ||||||
| chr2:55000210
|
G | C | 248 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(245): Show | 253 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.3014-12512C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000210 | ||||||
| chr2:55000239
|
C | G | 247 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(244): Show | 252 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.3014-12541G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000239 | ||||||
| chr2:55000247
|
G | T | 117 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(114): Show | 119 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.3014-12549C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000247 | ||||||
| chr2:55000322
|
C | T | 1 | a0001c0001t0010g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3014-12624G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000322 | ||||||
| chr2:55000346
|
T | TA | 7 | a0001c0001t0004g0079a0001c0001t0004g0193a0001c0001t0004g0194others(4): Show | 7 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3014-12649dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000346 | ||||||
| chr2:55000835
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3014-13137C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000835 | ||||||
| chr2:55000987
|
A | AT | 28 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(25): Show | 29 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3014-13290dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000987 | ||||||
| chr2:55001034
|
A | C | 6 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261others(3): Show | 6 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3014-13336T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001034 | ||||||
| chr2:55001256
|
C | T | 239 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(236): Show | 244 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3014-13558G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001256 | ||||||
| chr2:55001363
|
C | T | 239 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(236): Show | 244 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3014-13665G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001363 | ||||||
| chr2:55001429
|
T | A | 1 | a0002c0002t0003g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3014-13731A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001429 | ||||||
| chr2:55001437
|
T | C | 2 | a0001c0001t0002g0172a0001c0001t0002g0312 | 2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.3014-13739A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001437 | ||||||
| chr2:55001504
|
A | G | 1 | a0001c0001t0005g0299 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3014-13806T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001504 | ||||||
| chr2:55001585
|
T | C | 26 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(23): Show | 28 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.3014-13887A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001585 | ||||||
| chr2:55001587
|
G | C | 89 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(86): Show | 90 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.3014-13889C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001587 | ||||||
| chr2:55001699
|
T | C | 102 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0214others(99): Show | 103 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.3014-14001A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001699 | ||||||
| chr2:55001725
|
G | A | 245 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.3014-14027C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001725 | ||||||
| chr2:55001811
|
A | G | 51 | a0001c0001t0003g0128a0001c0001t0003g0129a0001c0001t0003g0130others(48): Show | 51 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3014-14113T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001811 | ||||||
| chr2:55001947
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3014-14249G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001947 | ||||||
| chr2:55001949
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3014-14251C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001949 | ||||||
| chr2:55001968
|
T | C | 1 | a0001c0001t0025g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3014-14270A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001968 | ||||||
| chr2:55001990
|
T | A | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-14292A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001990 | ||||||
| chr2:55001991
|
A | T | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-14293T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001991 | ||||||
| chr2:55002049
|
T | TTTTA | 92 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(89): Show | 93 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.3014-14355_3014-14 others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002049 | ||||||
| chr2:55002057
|
A | T | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3014-14359T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002057 | ||||||
| chr2:55002058
|
T | C | 6 | a0001c0008t0018g0067a0007c0007t0004g0062a0007c0007t0004g0063others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-14360A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002058 | ||||||
| chr2:55002173
|
C | T | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-14475G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002173 | ||||||
| chr2:55002203
|
C | T | 28 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(25): Show | 29 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3014-14505G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002203 | ||||||
| chr2:55002207
|
C | T | 28 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(25): Show | 29 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3014-14509G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002207 | ||||||
| chr2:55002231
|
T | C | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3014-14533A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002231 | ||||||
| chr2:55002237
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3014-14539A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002237 | ||||||
| chr2:55002351
|
G | T | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3014-14653C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002351 | ||||||
| chr2:55002364
|
T | C | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-14666A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002364 | ||||||
| chr2:55002372
|
T | C | 193 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(190): Show | 195 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.3014-14674A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002372 | ||||||
| chr2:55002383
|
A | G | 1 | a0001c0001t0025g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3014-14685T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002383 | ||||||
| chr2:55002691
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3014-14993G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002691 | ||||||
| chr2:55002719
|
C | A | 1 | a0002c0002t0003g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3014-15021G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002719 | ||||||
| chr2:55002806
|
T | C | 3 | a0001c0001t0003g0128a0001c0001t0003g0129a0002c0002t0019g0023 | 3 | HG03491.hp2 NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.3014-15108A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002806 | ||||||
| chr2:55002820
|
C | A | 4 | a0001c0001t0001g0241a0001c0001t0001g0246a0001c0001t0001g0257others(1): Show | 4 | NA18969.hp2 NA18991.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.3014-15122G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002820 | ||||||
| chr2:55002884
|
T | C | 11 | a0001c0001t0002g0146a0001c0001t0002g0159a0001c0001t0002g0190others(8): Show | 12 | HG01070.hp2 HG01071.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.3014-15186A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002884 | ||||||
| chr2:55002933
|
T | A | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-15235A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002933 | ||||||
| chr2:55002949
|
C | T | 88 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(85): Show | 89 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.3014-15251G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002949 | ||||||
| chr2:55002951
|
A | T | 88 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(85): Show | 89 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.3014-15253T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002951 | ||||||
| chr2:55003047
|
T | C | 4 | a0001c0001t0001g0216a0001c0001t0010g0273a0001c0001t0010g0275others(1): Show | 4 | HG02145.hp1 HG03834.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.3014-15349A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003047 | ||||||
| chr2:55003083
|
C | T | 239 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(236): Show | 244 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3014-15385G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003083 | ||||||
| chr2:55003278
|
T | C | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-15580A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003278 | ||||||
| chr2:55003410
|
C | T | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-15712G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003410 | ||||||
| chr2:55003906
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3014-16208A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003906 | ||||||
| chr2:55003918
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3014-16220G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003918 | ||||||
| chr2:55003982
|
T | A | 7 | a0001c0008t0018g0067a0007c0007t0004g0062a0007c0007t0004g0063others(4): Show | 7 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3014-16284A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003982 | ||||||
| chr2:55003991
|
A | C | 7 | a0001c0008t0018g0067a0007c0007t0004g0062a0007c0007t0004g0063others(4): Show | 7 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3014-16293T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003991 | ||||||
| chr2:55003997
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3014-16299C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003997 | ||||||
| chr2:55004160
|
T | G | 2 | a0001c0001t0002g0189a0001c0001t0002g0311 | 2 | NA18948.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.3014-16462A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004160 | ||||||
| chr2:55004220
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3014-16522G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004220 | ||||||
| chr2:55004293
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3014-16595C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004293 | ||||||
| chr2:55004312
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3014-16614A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004312 | ||||||
| chr2:55004379
|
G | A | 85 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(82): Show | 86 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.3014-16681C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004379 | ||||||
| chr2:55004427
|
G | A | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-16729C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004427 | ||||||
| chr2:55004521
|
T | A | 10 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(7): Show | 10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3014-16823A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004521 | ||||||
| chr2:55004562
|
G | A | 1 | a0001c0001t0005g0299 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3014-16864C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004562 | ||||||
| chr2:55004602
|
G | C | 1 | a0002c0002t0003g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3014-16904C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004602 | ||||||
| chr2:55004672
|
G | C | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-16974C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004672 | ||||||
| chr2:55004693
|
C | T | 38 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(35): Show | 39 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.3014-16995G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004693 | ||||||
| chr2:55004705
|
G | A | 58 | a0001c0001t0001g0214a0001c0001t0004g0077a0001c0001t0004g0079others(55): Show | 61 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.3014-17007C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004705 | ||||||
| chr2:55004792
|
T | C | 93 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(90): Show | 94 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.3014-17094A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004792 | ||||||
| chr2:55004806
|
T | C | 5 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261others(2): Show | 5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3014-17108A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004806 | ||||||
| chr2:55004848
|
C | T | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-17150G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004848 | ||||||
| chr2:55004859
|
G | C | 14 | a0002c0002t0001g0056a0002c0002t0003g0014a0002c0002t0003g0024others(11): Show | 14 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.3014-17161C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004859 | ||||||
| chr2:55005117
|
G | C | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-17419C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005117 | ||||||
| chr2:55005118
|
C | T | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-17420G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005118 | ||||||
| chr2:55005220
|
C | T | 6 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-17522G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005220 | ||||||
| chr2:55005561
|
G | A | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-17863C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005561 | ||||||
| chr2:55005649
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3014-17951A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005649 | ||||||
| chr2:55005814
|
G | C | 6 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(3): Show | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-18116C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005814 | ||||||
| chr2:55005859
|
A | G | 1 | a0001c0001t0005g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3014-18161T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005859 | ||||||
| chr2:55005973
|
A | T | 1 | a0001c0001t0012g0267 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3014-18275T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005973 | ||||||
| chr2:55006053
|
C | T | 2 | a0001c0001t0006g0309a0001c0001t0006g0310 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3014-18355G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006053 | ||||||
| chr2:55006054
|
G | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(32): Show | 36 | HG00735.hp2 HG01928.hp2 HG02080.hp1 others(33): Show |
intron_variant | MODIFIER | c.3014-18356C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006054 | ||||||
| chr2:55006197
|
T | G | 1 | a0002c0002t0003g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3014-18499A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006197 | ||||||
| chr2:55006222
|
A | C | 1 | a0001c0001t0002g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3014-18524T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006222 | ||||||
| chr2:55006392
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3013+18694G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006392 | ||||||
| chr2:55006412
|
G | A | 2 | a0001c0001t0005g0290a0001c0001t0005g0291 | 2 | HG00099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.3013+18674C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006412 | ||||||
| chr2:55006688
|
A | G | 1 | a0007c0007t0004g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3013+18398T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006688 | ||||||
| chr2:55006806
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3013+18280G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006806 | ||||||
| chr2:55006806
|
C | G | 3 | a0001c0001t0012g0264a0001c0001t0012g0267a0001c0001t0012g0268 | 3 | HG02132.hp2 NA18986.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3013+18280G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006806 | ||||||
| chr2:55007126
|
C | A | 7 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(4): Show | 7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3013+17960G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007126 | ||||||
| chr2:55007145
|
T | C | 2 | a0001c0001t0001g0272a0001c0017t0001g0265 | 2 | HG01496.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.3013+17941A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007145 | ||||||
| chr2:55007168
|
C | T | 1 | a0014c0018t0020g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3013+17918G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007168 | ||||||
| chr2:55007176
|
T | C | 27 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(24): Show | 29 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.3013+17910A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007176 | ||||||
| chr2:55007182
|
G | T | 1 | a0001c0001t0013g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3013+17904C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007182 | ||||||
| chr2:55007209
|
C | T | 5 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0098others(2): Show | 5 | HG01081.hp2 HG01257.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013+17877G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007209 | ||||||
| chr2:55007335
|
C | A | 17 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(14): Show | 17 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.3013+17751G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007335 | ||||||
| chr2:55007453
|
T | C | 1 | a0010c0024t0006g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3013+17633A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007453 | ||||||
| chr2:55007794
|
A | G | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3013+17292T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007794 | ||||||
| chr2:55008110
|
G | A | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+16976C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008110 | ||||||
| chr2:55008142
|
A | AAC | 55 | a0001c0001t0001g0078a0001c0001t0001g0086a0001c0001t0001g0087others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.3013+16942_3013+16 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008142
|
A | AACAC | 16 | a0001c0001t0001g0083a0001c0001t0001g0093a0001c0001t0001g0096others(13): Show | 17 | HG00423.hp1 HG01167.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.3013+16940_3013+16 others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008142
|
A | AACACAC | 41 | a0001c0001t0001g0110a0001c0001t0001g0126a0001c0001t0001g0223others(38): Show | 41 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(38): Show |
intron_variant | MODIFIER | c.3013+16938_3013+16 others(12): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008142
|
A | AACACACA others(1): Show |
43 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0075others(40): Show | 45 | HG00323.hp2 HG00544.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.3013+16936_3013+16 others(14): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008142
|
A | AACACACA others(3): Show |
48 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0114others(45): Show | 49 | HG00558.hp2 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.3013+16934_3013+16 others(16): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008142
|
A | AACACACA others(5): Show |
14 | a0001c0001t0001g0101a0001c0001t0001g0104a0001c0001t0003g0128others(11): Show | 15 | HG00642.hp1 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.3013+16932_3013+16 others(18): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008142
|
A | AACACACA others(7): Show |
3 | a0001c0001t0007g0335a0001c0008t0018g0067a0002c0011t0003g0046 | 3 | HG01943.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3013+16930_3013+16 others(20): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008142
|
A | AACACACA others(9): Show |
1 | a0002c0002t0003g0044 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3013+16928_3013+16 others(22): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008142
|
A | ACACAC | 3 | a0001c0001t0001g0270a0001c0001t0002g0070a0001c0001t0004g0079 | 3 | HG02165.hp2 HG02615.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.3013+16943_3013+16 others(11): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008142
|
A | ACACACAC others(4): Show |
2 | a0002c0002t0003g0020a0003c0003t0014g0072 | 2 | HG00544.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3013+16943_3013+16 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | ||||||
| chr2:55008237
|
T | C | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+16849A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008237 | ||||||
| chr2:55008367
|
G | C | 3 | a0001c0001t0002g0292a0001c0010t0002g0320a0001c0010t0002g0321 | 3 | HG01109.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3013+16719C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008367 | ||||||
| chr2:55008731
|
T | C | 1 | a0001c0001t0013g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3013+16355A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008731 | ||||||
| chr2:55008748
|
CTTAAG | C | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+16333_3013+16 others(11): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008748 | ||||||
| chr2:55008830
|
T | C | 33 | a0001c0001t0001g0214a0001c0001t0005g0011a0001c0001t0005g0277others(30): Show | 36 | HG00099.hp2 HG00738.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.3013+16256A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008830 | ||||||
| chr2:55008954
|
A | G | 4 | a0006c0006t0002g0003a0006c0006t0002g0301a0006c0006t0002g0302others(1): Show | 6 | HG00738.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+16132T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008954 | ||||||
| chr2:55009039
|
A | AT | 97 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(94): Show | 98 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.3013+16046dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009039 | ||||||
| chr2:55009224
|
C | T | 72 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(69): Show | 73 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.3013+15862G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009224 | ||||||
| chr2:55009312
|
T | C | 96 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(93): Show | 97 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.3013+15774A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009312 | ||||||
| chr2:55009438
|
G | T | 1 | a0001c0001t0002g0132 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3013+15648C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009438 | ||||||
| chr2:55009490
|
T | G | 1 | a0001c0001t0001g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3013+15596A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009490 | ||||||
| chr2:55009526
|
G | A | 3 | a0001c0001t0010g0273a0001c0001t0010g0275a0001c0001t0010g0276 | 3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3013+15560C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009526 | ||||||
| chr2:55009732
|
G | A | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+15354C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009732 | ||||||
| chr2:55009863
|
GAC | G | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15221_3013+15 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009863 | ||||||
| chr2:55009866
|
T | G | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15220A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009866 | ||||||
| chr2:55009868
|
A | T | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15218T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009868 | ||||||
| chr2:55009869
|
A | T | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15217T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009869 | ||||||
| chr2:55009870
|
A | T | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15216T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009870 | ||||||
| chr2:55009873
|
A | G | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15213T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009873 | ||||||
| chr2:55009880
|
C | T | 1 | a0002c0002t0003g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3013+15206G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009880 | ||||||
| chr2:55009913
|
T | G | 97 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(94): Show | 98 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.3013+15173A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009913 | ||||||
| chr2:55010131
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3013+14955C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55010131 | ||||||
| chr2:55010161
|
T | C | 1 | a0001c0001t0005g0285 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3013+14925A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55010161 | ||||||
| chr2:55010577
|
A | G | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3013+14509T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55010577 | ||||||
| chr2:55010770
|
A | C | 6 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(3): Show | 6 | HG02647.hp2 HG02970.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+14316T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55010770 | ||||||
| chr2:55011096
|
A | C | 1 | a0001c0001t0001g0227 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3013+13990T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011096 | ||||||
| chr2:55011202
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3013+13884G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011202 | ||||||
| chr2:55011293
|
C | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(64): Show | 68 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.3013+13793G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011293 | ||||||
| chr2:55011371
|
T | A | 1 | a0002c0002t0003g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3013+13715A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011371 | ||||||
| chr2:55011404
|
T | C | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3013+13682A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011404 | ||||||
| chr2:55011452
|
C | G | 1 | a0001c0008t0008g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3013+13634G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011452 | ||||||
| chr2:55011458
|
C | T | 2 | a0003c0003t0004g0317a0003c0003t0004g0318 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3013+13628G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011458 | ||||||
| chr2:55011521
|
G | A | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3013+13565C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011521 | ||||||
| chr2:55011540
|
C | T | 3 | a0001c0001t0012g0264a0001c0001t0012g0267a0001c0001t0012g0268 | 3 | HG02132.hp2 NA18986.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3013+13546G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011540 | ||||||
| chr2:55011541
|
G | A | 56 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(53): Show | 57 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3013+13545C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011541 | ||||||
| chr2:55011620
|
C | G | 82 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(79): Show | 85 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.3013+13466G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011620 | ||||||
| chr2:55011715
|
C | G | 163 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(160): Show | 165 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.3013+13371G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011715 | ||||||
| chr2:55011723
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3013+13363A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011723 | ||||||
| chr2:55011748
|
G | A | 1 | a0001c0001t0003g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3013+13338C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011748 | ||||||
| chr2:55011754
|
G | A | 3 | a0001c0001t0010g0273a0001c0001t0010g0275a0001c0001t0010g0276 | 3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3013+13332C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011754 | ||||||
| chr2:55011770
|
T | C | 1 | a0002c0002t0003g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3013+13316A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011770 | ||||||
| chr2:55011914
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3013+13172A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011914 | ||||||
| chr2:55011944
|
A | G | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3013+13142T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011944 | ||||||
| chr2:55012066
|
G | T | 220 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.3013+13020C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012066 | ||||||
| chr2:55012200
|
T | A | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+12886A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012200 | ||||||
| chr2:55012274
|
T | C | 187 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(184): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.3013+12812A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012274 | ||||||
| chr2:55012372
|
C | A | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+12714G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012372 | ||||||
| chr2:55012401
|
A | T | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+12685T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012401 | ||||||
| chr2:55012415
|
AC | A | 15 | a0001c0001t0001g0216a0001c0001t0002g0274a0001c0001t0007g0332others(12): Show | 15 | HG00140.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.3013+12670delG | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012415 | ||||||
| chr2:55012591
|
T | C | 10 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(7): Show | 10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3013+12495A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012591 | ||||||
| chr2:55012682
|
A | G | 7 | a0001c0001t0004g0138a0001c0001t0004g0197a0001c0001t0004g0199others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3013+12404T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012682 | ||||||
| chr2:55012772
|
A | G | 2 | a0001c0001t0005g0287a0001c0001t0005g0288 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3013+12314T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012772 | ||||||
| chr2:55012890
|
A | C | 247 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(244): Show | 252 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.3013+12196T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012890 | ||||||
| chr2:55013015
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3013+12071A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013015 | ||||||
| chr2:55013210
|
G | A | 1 | a0002c0002t0003g0052 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3013+11876C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013210 | ||||||
| chr2:55013228
|
T | C | 10 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(7): Show | 10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3013+11858A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013228 | ||||||
| chr2:55013251
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3013+11835A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013251 | ||||||
| chr2:55013276
|
C | T | 1 | a0001c0001t0010g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3013+11810G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013276 | ||||||
| chr2:55013463
|
C | A | 76 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(73): Show | 77 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.3013+11623G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013463 | ||||||
| chr2:55013503
|
C | T | 1 | a0001c0001t0013g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3013+11583G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013503 | ||||||
| chr2:55013554
|
A | T | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+11532T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013554 | ||||||
| chr2:55013599
|
G | GT | 12 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0001g0124others(9): Show | 12 | HG01978.hp2 HG02055.hp2 HG03654.hp2 others(9): Show |
intron_variant | MODIFIER | c.3013+11486dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013599 | ||||||
| chr2:55013608
|
T | G | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+11478A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013608 | ||||||
| chr2:55013608
|
TG | T | 159 | a0001c0001t0001g0010a0001c0001t0001g0099a0001c0001t0001g0113others(156): Show | 165 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(162): Show |
intron_variant | MODIFIER | c.3013+11477delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013608 | ||||||
| chr2:55013609
|
G | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(74): Show | 78 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3013+11477C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013609 | ||||||
| chr2:55013610
|
G | T | 22 | a0001c0001t0001g0099a0001c0001t0001g0216a0001c0001t0007g0332others(19): Show | 22 | HG01167.hp1 HG02109.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.3013+11476C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013610 | ||||||
| chr2:55013622
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(88): Show | 92 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.3013+11464C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013622 | ||||||
| chr2:55013627
|
A | AG | 11 | a0001c0001t0001g0263a0001c0001t0002g0152a0001c0001t0002g0158others(8): Show | 11 | HG01109.hp1 HG01175.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.3013+11458dupC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013627 | ||||||
| chr2:55013678
|
T | TTAGATTT others(9): Show |
1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+11407_3013+11 others(22): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013678 | ||||||
| chr2:55013748
|
T | G | 1 | a0001c0001t0017g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3013+11338A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013748 | ||||||
| chr2:55014080
|
A | T | 248 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(245): Show | 253 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.3013+11006T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014080 | ||||||
| chr2:55014159
|
A | C | 4 | a0001c0001t0009g0082a0004c0005t0001g0323a0004c0005t0001g0325others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3013+10927T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014159 | ||||||
| chr2:55014279
|
G | A | 2 | a0005c0004t0002g0009a0005c0004t0002g0137 | 3 | HG01070.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.3013+10807C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014279 | ||||||
| chr2:55014522
|
A | AT | 123 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(120): Show | 125 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.3013+10563dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014522 | ||||||
| chr2:55014550
|
G | T | 238 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(235): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.3013+10536C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014550 | ||||||
| chr2:55014575
|
T | A | 77 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(74): Show | 78 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3013+10511A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014575 | ||||||
| chr2:55014613
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3013+10473C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014613 | ||||||
| chr2:55014866
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3013+10220G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014866 | ||||||
| chr2:55015059
|
G | A | 3 | a0001c0001t0012g0264a0001c0001t0012g0267a0001c0001t0012g0268 | 3 | HG02132.hp2 NA18986.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3013+10027C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015059 | ||||||
| chr2:55015133
|
C | T | 1 | a0002c0002t0003g0036 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3013+9953G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015133 | ||||||
| chr2:55015245
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3013+9841G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015245 | ||||||
| chr2:55015320
|
C | T | 98 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(95): Show | 99 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.3013+9766G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015320 | ||||||
| chr2:55015327
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0140a0001c0001t0002g0141others(2): Show | 6 | HG00438.hp2 HG02080.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+9759C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015327 | ||||||
| chr2:55015328
|
G | A | 2 | a0005c0004t0002g0009a0005c0004t0002g0137 | 3 | HG01070.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.3013+9758C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015328 | ||||||
| chr2:55015555
|
G | T | 1 | a0001c0001t0007g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3013+9531C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015555 | ||||||
| chr2:55015579
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0307 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3013+9507A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015579 | ||||||
| chr2:55015737
|
A | G | 1 | a0001c0001t0005g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3013+9349T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015737 | ||||||
| chr2:55015859
|
T | C | 6 | a0001c0001t0004g0079a0001c0001t0004g0193a0001c0001t0004g0194others(3): Show | 6 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3013+9227A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015859 | ||||||
| chr2:55016068
|
T | A | 31 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(28): Show | 35 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.3013+9018A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016068 | ||||||
| chr2:55016301
|
G | A | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3013+8785C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016301 | ||||||
| chr2:55016347
|
C | T | 4 | a0001c0001t0009g0082a0004c0005t0001g0323a0004c0005t0001g0325others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3013+8739G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016347 | ||||||
| chr2:55016348
|
C | G | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3013+8738G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016348 | ||||||
| chr2:55016490
|
C | T | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+8596G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016490 | ||||||
| chr2:55016534
|
G | C | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3013+8552C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016534 | ||||||
| chr2:55016549
|
A | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(35): Show | 39 | HG00735.hp2 HG01928.hp2 HG02080.hp1 others(36): Show |
intron_variant | MODIFIER | c.3013+8537T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016549 | ||||||
| chr2:55016628
|
GAATAA | G | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+8453_3013+845 others(9): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016628 | ||||||
| chr2:55016665
|
C | A | 1 | a0001c0001t0001g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3013+8421G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016665 | ||||||
| chr2:55016667
|
G | C | 5 | a0001c0001t0001g0216a0001c0001t0002g0274a0001c0001t0010g0273others(2): Show | 5 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013+8419C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016667 | ||||||
| chr2:55016746
|
T | A | 1 | a0002c0002t0003g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3013+8340A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016746 | ||||||
| chr2:55016810
|
C | A | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+8276G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016810 | ||||||
| chr2:55017064
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0140a0001c0001t0002g0141others(2): Show | 6 | HG00438.hp2 HG02080.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+8022G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017064 | ||||||
| chr2:55017262
|
C | G | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+7824G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017262 | ||||||
| chr2:55017266
|
G | A | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3013+7820C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017266 | ||||||
| chr2:55017302
|
G | A | 220 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.3013+7784C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017302 | ||||||
| chr2:55017357
|
A | G | 3 | a0001c0001t0012g0264a0001c0001t0012g0267a0001c0001t0012g0268 | 3 | HG02132.hp2 NA18986.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3013+7729T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017357 | ||||||
| chr2:55017360
|
T | C | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+7726A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017360 | ||||||
| chr2:55017402
|
A | C | 80 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(77): Show | 81 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3013+7684T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017402 | ||||||
| chr2:55017544
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3013+7542C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017544 | ||||||
| chr2:55017566
|
C | T | 1 | a0001c0001t0002g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3013+7520G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017566 | ||||||
| chr2:55017609
|
A | G | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3013+7477T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017609 | ||||||
| chr2:55017695
|
C | A | 26 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(23): Show | 28 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.3013+7391G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017695 | ||||||
| chr2:55017846
|
C | T | 29 | a0001c0001t0001g0214a0001c0001t0005g0011a0001c0001t0005g0277others(26): Show | 30 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.3013+7240G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017846 | ||||||
| chr2:55018028
|
G | A | 1 | a0001c0001t0010g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3013+7058C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018028 | ||||||
| chr2:55018041
|
T | C | 194 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(191): Show | 196 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.3013+7045A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018041 | ||||||
| chr2:55018084
|
A | G | 292 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(289): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.3013+7002T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018084 | ||||||
| chr2:55018143
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3013+6943A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018143 | ||||||
| chr2:55018147
|
T | C | 5 | a0001c0001t0001g0216a0001c0001t0002g0274a0001c0001t0010g0273others(2): Show | 5 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013+6939A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018147 | ||||||
| chr2:55018238
|
T | C | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3013+6848A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018238 | ||||||
| chr2:55018531
|
GT | G | 55 | a0001c0001t0001g0214a0001c0001t0004g0077a0001c0001t0004g0079others(52): Show | 58 | HG00099.hp2 HG01109.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.3013+6554delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018531 | ||||||
| chr2:55018613
|
T | C | 1 | a0001c0001t0005g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3013+6473A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018613 | ||||||
| chr2:55018719
|
A | G | 1 | a0002c0002t0011g0018 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3013+6367T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018719 | ||||||
| chr2:55019066
|
C | G | 31 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(28): Show | 35 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.3013+6020G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019066 | ||||||
| chr2:55019167
|
T | C | 31 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(28): Show | 35 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.3013+5919A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019167 | ||||||
| chr2:55019287
|
A | G | 63 | a0001c0001t0001g0214a0001c0001t0004g0077a0001c0001t0004g0079others(60): Show | 68 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.3013+5799T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019287 | ||||||
| chr2:55019306
|
G | T | 11 | a0001c0001t0002g0008a0001c0001t0002g0134a0001c0001t0002g0155others(8): Show | 12 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.3013+5780C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019306 | ||||||
| chr2:55019348
|
G | A | 1 | a0001c0001t0005g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3013+5738C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019348 | ||||||
| chr2:55019415
|
C | T | 250 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(247): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.3013+5671G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019415 | ||||||
| chr2:55019460
|
C | T | 31 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(28): Show | 35 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.3013+5626G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019460 | ||||||
| chr2:55019603
|
C | T | 31 | a0001c0001t0001g0214a0001c0001t0005g0011a0001c0001t0005g0277others(28): Show | 32 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.3013+5483G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019603 | ||||||
| chr2:55019651
|
G | A | 1 | a0001c0001t0002g0146 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3013+5435C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019651 | ||||||
| chr2:55019729
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0188 | 2 | HG02622.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.3013+5357A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019729 | ||||||
| chr2:55019780
|
T | C | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201 | 3 | HG03041.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3013+5306A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019780 | ||||||
| chr2:55019935
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3013+5151A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019935 | ||||||
| chr2:55020121
|
C | T | 69 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(66): Show | 70 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.3013+4965G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020121 | ||||||
| chr2:55020122
|
G | A | 8 | a0001c0001t0004g0138a0001c0001t0004g0197a0001c0001t0004g0198others(5): Show | 8 | HG01891.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3013+4964C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020122 | ||||||
| chr2:55020130
|
C | G | 1 | a0004c0005t0001g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3013+4956G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020130 | ||||||
| chr2:55020327
|
G | T | 79 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(76): Show | 80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3013+4759C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020327 | ||||||
| chr2:55020341
|
T | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(186): Show | 191 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.3013+4745A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020341 | ||||||
| chr2:55020363
|
T | C | 5 | a0001c0001t0001g0216a0001c0001t0002g0274a0001c0001t0010g0273others(2): Show | 5 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013+4723A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020363 | ||||||
| chr2:55020421
|
G | GA | 189 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(186): Show | 191 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.3013+4664dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020421 | ||||||
| chr2:55020477
|
A | ACTAC | 89 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(86): Show | 90 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.3013+4605_3013+460 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020477 | ||||||
| chr2:55020618
|
C | T | 1 | a0001c0001t0002g0190 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3013+4468G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020618 | ||||||
| chr2:55020707
|
C | G | 7 | a0001c0001t0004g0079a0001c0001t0004g0193a0001c0001t0004g0194others(4): Show | 7 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3013+4379G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020707 | ||||||
| chr2:55020743
|
C | A | 4 | a0001c0001t0002g0274a0001c0001t0010g0273a0001c0001t0010g0275others(1): Show | 4 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3013+4343G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020743 | ||||||
| chr2:55020818
|
A | G | 249 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(246): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3013+4268T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020818 | ||||||
| chr2:55021043
|
T | C | 4 | a0001c0001t0002g0274a0001c0001t0010g0273a0001c0001t0010g0275others(1): Show | 4 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3013+4043A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021043 | ||||||
| chr2:55021221
|
T | G | 195 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(192): Show | 199 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.3013+3865A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021221 | ||||||
| chr2:55021325
|
G | A | 1 | a0001c0001t0005g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3013+3761C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021325 | ||||||
| chr2:55021391
|
G | GC | 40 | a0001c0001t0001g0214a0001c0001t0005g0011a0001c0001t0005g0277others(37): Show | 41 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.3013+3694dupG | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021391 | ||||||
| chr2:55021394
|
C | CG | 89 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0219others(86): Show | 90 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.3013+3691_3013+369 others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021394 | ||||||
| chr2:55021400
|
G | C | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3013+3686C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021400 | ||||||
| chr2:55021401
|
C | G | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3013+3685G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021401 | ||||||
| chr2:55021403
|
A | C | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3013+3683T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021403 | ||||||
| chr2:55021466
|
C | CT | 8 | a0001c0001t0002g0076a0001c0001t0002g0222a0002c0002t0001g0049others(5): Show | 10 | HG00609.hp1 HG00738.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.3013+3619dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021466 | ||||||
| chr2:55021466
|
CT | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(79): Show | 83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3013+3619delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021466 | ||||||
| chr2:55021512
|
G | A | 10 | a0002c0002t0001g0049a0002c0002t0003g0013a0002c0002t0003g0015others(7): Show | 10 | HG01070.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3013+3574C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021512 | ||||||
| chr2:55021543
|
G | C | 1 | a0001c0001t0002g0181 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3013+3543C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021543 | ||||||
| chr2:55021593
|
G | C | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+3493C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021593 | ||||||
| chr2:55021682
|
T | C | 35 | a0001c0001t0001g0214a0001c0001t0005g0011a0001c0001t0005g0277others(32): Show | 36 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3013+3404A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021682 | ||||||
| chr2:55021721
|
A | G | 35 | a0001c0001t0001g0214a0001c0001t0005g0011a0001c0001t0005g0277others(32): Show | 36 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3013+3365T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021721 | ||||||
| chr2:55021829
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3013+3257G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021829 | ||||||
| chr2:55022068
|
A | C | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+3018T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022068 | ||||||
| chr2:55022220
|
A | G | 2 | a0001c0001t0009g0149a0001c0001t0009g0316 | 2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3013+2866T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022220 | ||||||
| chr2:55022235
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3013+2851G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022235 | ||||||
| chr2:55022346
|
T | C | 15 | a0001c0001t0002g0159a0001c0001t0002g0190a0001c0001t0009g0149others(12): Show | 18 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.3013+2740A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022346 | ||||||
| chr2:55022554
|
A | G | 1 | a0001c0001t0005g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3013+2532T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022554 | ||||||
| chr2:55022896
|
A | AAC | 18 | a0001c0001t0002g0081a0001c0001t0002g0133a0001c0001t0002g0152others(15): Show | 18 | HG01069.hp2 HG01071.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.3013+2188_3013+218 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACAC | 10 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0274others(7): Show | 10 | HG00140.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3013+2186_3013+218 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACAC | 3 | a0001c0001t0005g0278a0001c0001t0010g0273a0001c0008t0018g0067 | 3 | HG02647.hp1 HG02809.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.3013+2184_3013+218 others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(1): Show |
16 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0206others(13): Show | 16 | HG00099.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.3013+2182_3013+218 others(12): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(3): Show |
3 | a0001c0001t0001g0093a0001c0001t0001g0262a0001c0017t0001g0265 | 3 | HG01496.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3013+2180_3013+218 others(14): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(5): Show |
45 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0078others(42): Show | 46 | HG00558.hp2 HG00741.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.3013+2178_3013+218 others(16): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(7): Show |
15 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0103others(12): Show | 15 | HG00323.hp2 HG00423.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.3013+2176_3013+218 others(18): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(9): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0087a0001c0001t0001g0121others(1): Show | 4 | HG00544.hp1 HG02559.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3013+2174_3013+218 others(20): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(11): Show |
29 | a0001c0001t0001g0010a0001c0001t0001g0219a0001c0001t0001g0223others(26): Show | 30 | HG00735.hp2 HG01070.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.3013+2172_3013+218 others(22): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(13): Show |
16 | a0001c0001t0001g0120a0001c0001t0001g0243a0001c0001t0001g0249others(13): Show | 16 | HG00735.hp1 HG00738.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.3013+2170_3013+218 others(24): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(15): Show |
25 | a0001c0001t0001g0225a0001c0001t0001g0237a0001c0001t0001g0238others(22): Show | 25 | HG00642.hp1 HG01167.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.3013+2168_3013+218 others(26): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(17): Show |
10 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0234others(7): Show | 10 | HG00544.hp2 HG01074.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.3013+2166_3013+218 others(28): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(19): Show |
6 | a0001c0001t0001g0226a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG02148.hp1 NA18952.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+2164_3013+218 others(30): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | AACACACA others(21): Show |
1 | a0012c0014t0001g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3013+2162_3013+218 others(32): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022896
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3013+2189_3013+219 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | ||||||
| chr2:55022930
|
C | CACACACA others(6): Show |
1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3013+2155_3013+215 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022930 | ||||||
| chr2:55022930
|
C | CACACACA others(12): Show |
2 | a0001c0001t0001g0251a0002c0002t0003g0053 | 2 | HG04184.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.3013+2155_3013+215 others(23): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022930 | ||||||
| chr2:55022985
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3013+2101T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022985 | ||||||
| chr2:55023258
|
G | T | 1 | a0001c0001t0007g0333 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3013+1828C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55023258 | ||||||
| chr2:55023485
|
A | G | 1 | a0002c0002t0003g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3013+1601T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55023485 | ||||||
| chr2:55023610
|
G | A | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.3013+1476C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55023610 | ||||||
| chr2:55024071
|
T | C | 32 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0005g0011others(29): Show | 33 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.3013+1015A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024071 | ||||||
| chr2:55024089
|
T | C | 1 | a0001c0001t0012g0268 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3013+997A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024089 | ||||||
| chr2:55024095
|
C | T | 30 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(27): Show | 32 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.3013+991G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024095 | ||||||
| chr2:55024216
|
C | T | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3013+870G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024216 | ||||||
| chr2:55024238
|
G | A | 134 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(131): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.3013+848C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024238 | ||||||
| chr2:55024331
|
G | A | 19 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(16): Show | 19 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.3013+755C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024331 | ||||||
| chr2:55024375
|
C | G | 50 | a0001c0001t0003g0128a0001c0001t0003g0129a0001c0001t0003g0130others(47): Show | 50 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.3013+711G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024375 | ||||||
| chr2:55024415
|
C | T | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3013+671G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024415 | ||||||
| chr2:55024468
|
A | T | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3013+618T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024468 | ||||||
| chr2:55024505
|
A | G | 4 | a0001c0001t0002g0274a0001c0001t0010g0273a0001c0001t0010g0275others(1): Show | 4 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3013+581T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024505 | ||||||
| chr2:55024585
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0227a0001c0001t0001g0228others(3): Show | 7 | NA18951.hp1 NA18971.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.3013+501A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024585 | ||||||
| chr2:55024654
|
A | G | 1 | a0001c0001t0010g0273 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3013+432T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024654 | ||||||
| chr2:55024705
|
T | C | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3013+381A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024705 | ||||||
| chr2:55024975
|
A | C | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+111T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024975 | ||||||
| chr2:55025041
|
C | T | 23 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(20): Show | 25 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.3013+45G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55025041 | ||||||
| chr2:55025058
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3013+28C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55025058 | ||||||
| chr2:55025078
|
T | G | 35 | a0001c0001t0001g0216a0001c0001t0002g0274a0001c0001t0005g0011others(32): Show | 36 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(33): Show |
splice_region_variant&intron_variant | LOW | c.3013+8A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55025078 | ||||||
| chr2:55027567
|
G | A | 7 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(4): Show | 7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-82C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027567 | ||||||
| chr2:55027585
|
T | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0219a0001c0001t0001g0223others(16): Show | 20 | HG00735.hp2 HG01928.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.614-100A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027585 | ||||||
| chr2:55027667
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.614-182A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027667 | ||||||
| chr2:55027678
|
CAT | C | 17 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(14): Show | 17 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.614-195_614-194del others(2): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027678 | ||||||
| chr2:55027717
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.614-232C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027717 | ||||||
| chr2:55027970
|
G | A | 2 | a0001c0001t0002g0069a0001c0001t0002g0070 | 2 | HG02040.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.613+194C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027970 | ||||||
| chr2:55028523
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.557-303T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028523 | ||||||
| chr2:55028587
|
C | T | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.557-367G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028587 | ||||||
| chr2:55028660
|
C | T | 3 | a0001c0001t0002g0274a0001c0001t0010g0273a0001c0001t0010g0275 | 3 | HG00140.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.557-440G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028660 | ||||||
| chr2:55028734
|
C | T | 288 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(285): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.557-514G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028734 | ||||||
| chr2:55028787
|
CA | C | 227 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.557-568delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028787 | ||||||
| chr2:55028799
|
A | T | 247 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(244): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.557-579T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028799 | ||||||
| chr2:55028863
|
A | G | 1 | a0001c0001t0022g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.557-643T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028863 | ||||||
| chr2:55028962
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.557-742T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028962 | ||||||
| chr2:55029007
|
T | C | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.557-787A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029007 | ||||||
| chr2:55029105
|
AC | A | 5 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0023t0001g0322others(2): Show | 5 | HG02040.hp2 HG02165.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-886delG | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029105 | ||||||
| chr2:55029277
|
A | C | 1 | a0001c0001t0002g0070 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.557-1057T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029277 | ||||||
| chr2:55029518
|
T | C | 1 | a0001c0001t0006g0304 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.557-1298A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029518 | ||||||
| chr2:55029591
|
A | G | 4 | a0002c0002t0003g0027a0002c0002t0003g0028a0002c0002t0003g0029others(1): Show | 4 | NA18952.hp1 NA18960.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-1371T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029591 | ||||||
| chr2:55030062
|
T | C | 2 | a0001c0001t0005g0287a0001c0001t0005g0288 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.557-1842A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030062 | ||||||
| chr2:55030099
|
G | C | 1 | a0013c0019t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.557-1879C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030099 | ||||||
| chr2:55030149
|
T | C | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-1929A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030149 | ||||||
| chr2:55030273
|
T | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(79): Show | 83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.557-2053A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030273 | ||||||
| chr2:55030351
|
T | C | 1 | a0001c0001t0002g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.557-2131A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030351 | ||||||
| chr2:55030450
|
G | T | 29 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(26): Show | 30 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.557-2230C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030450 | ||||||
| chr2:55030453
|
T | C | 1 | a0001c0001t0005g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.557-2233A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030453 | ||||||
| chr2:55030541
|
C | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(60): Show | 64 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.557-2321G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030541 | ||||||
| chr2:55031018
|
AC | A | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-2799delG | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031018 | ||||||
| chr2:55031059
|
C | T | 19 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(16): Show | 19 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.557-2839G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031059 | ||||||
| chr2:55031241
|
C | T | 19 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(16): Show | 19 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.557-3021G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031241 | ||||||
| chr2:55031421
|
A | T | 1 | a0001c0001t0001g0234 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.557-3201T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031421 | ||||||
| chr2:55031568
|
C | G | 59 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(56): Show | 60 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.557-3348G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031568 | ||||||
| chr2:55031710
|
C | G | 4 | a0002c0002t0003g0027a0002c0002t0003g0028a0002c0002t0003g0029others(1): Show | 4 | NA18952.hp1 NA18960.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-3490G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031710 | ||||||
| chr2:55031715
|
T | C | 2 | a0001c0001t0017g0313a0002c0002t0002g0060 | 2 | HG03195.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.557-3495A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031715 | ||||||
| chr2:55031789
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.557-3569C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031789 | ||||||
| chr2:55031815
|
C | A | 1 | a0006c0006t0002g0302 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.557-3595G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031815 | ||||||
| chr2:55031993
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.557-3773A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031993 | ||||||
| chr2:55032023
|
T | C | 1 | a0001c0001t0007g0333 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.557-3803A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032023 | ||||||
| chr2:55032056
|
C | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.557-3836G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032056 | ||||||
| chr2:55032133
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.557-3913A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032133 | ||||||
| chr2:55032159
|
C | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.557-3939G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032159 | ||||||
| chr2:55032544
|
A | G | 19 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(16): Show | 19 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.557-4324T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032544 | ||||||
| chr2:55032602
|
T | A | 1 | a0001c0001t0002g0182 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.557-4382A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032602 | ||||||
| chr2:55032603
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.557-4383A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032603 | ||||||
| chr2:55032612
|
A | T | 94 | a0001c0001t0001g0010a0001c0001t0001g0219a0001c0001t0001g0223others(91): Show | 95 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.557-4392T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032612 | ||||||
| chr2:55032785
|
T | C | 1 | a0001c0001t0002g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.557-4565A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032785 | ||||||
| chr2:55032791
|
G | A | 3 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261 | 3 | HG02818.hp2 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.557-4571C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032791 | ||||||
| chr2:55032837
|
T | G | 1 | a0001c0001t0002g0183 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.557-4617A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032837 | ||||||
| chr2:55033050
|
T | TA | 63 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(60): Show | 66 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.557-4831dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033050 | ||||||
| chr2:55033050
|
TA | T | 7 | a0001c0001t0001g0084a0001c0001t0001g0226a0001c0001t0002g0132others(4): Show | 7 | HG00323.hp1 HG01257.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.557-4831delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033050 | ||||||
| chr2:55033057
|
A | G | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.557-4837T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033057 | ||||||
| chr2:55033161
|
A | C | 1 | a0007c0007t0004g0062 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.557-4941T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033161 | ||||||
| chr2:55033277
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.557-5057A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033277 | ||||||
| chr2:55033426
|
C | G | 14 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0002g0190others(11): Show | 14 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.557-5206G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033426 | ||||||
| chr2:55033498
|
T | G | 1 | a0001c0001t0002g0222 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.557-5278A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033498 | ||||||
| chr2:55033511
|
G | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(51): Show | 55 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.557-5291C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033511 | ||||||
| chr2:55033596
|
G | A | 8 | a0001c0001t0002g0190a0001c0001t0007g0332a0001c0001t0007g0333others(5): Show | 8 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-5376C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033596 | ||||||
| chr2:55033807
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.557-5587A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033807 | ||||||
| chr2:55033810
|
G | A | 29 | a0001c0001t0005g0011a0001c0001t0005g0278a0001c0001t0005g0279others(26): Show | 30 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.557-5590C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033810 | ||||||
| chr2:55033921
|
T | C | 1 | a0002c0002t0003g0019 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.557-5701A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033921 | ||||||
| chr2:55033955
|
C | T | 1 | a0001c0001t0009g0316 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.557-5735G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033955 | ||||||
| chr2:55034161
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.557-5941A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034161 | ||||||
| chr2:55034351
|
C | A | 239 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(236): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.557-6131G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034351 | ||||||
| chr2:55034496
|
T | C | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.557-6276A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034496 | ||||||
| chr2:55034523
|
T | C | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.557-6303A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034523 | ||||||
| chr2:55034603
|
T | A | 1 | a0001c0001t0009g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.557-6383A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034603 | ||||||
| chr2:55034795
|
T | A | 248 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(245): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.557-6575A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034795 | ||||||
| chr2:55035002
|
A | G | 2 | a0001c0001t0002g0152a0001c0001t0024g0154 | 2 | HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.557-6782T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035002 | ||||||
| chr2:55035023
|
C | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(76): Show | 80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.557-6803G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035023 | ||||||
| chr2:55035174
|
G | A | 5 | a0001c0001t0001g0216a0001c0001t0002g0274a0001c0001t0010g0273others(2): Show | 5 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-6954C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035174 | ||||||
| chr2:55035229
|
T | G | 1 | a0001c0001t0002g0152 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.557-7009A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035229 | ||||||
| chr2:55035368
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.557-7148C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035368 | ||||||
| chr2:55035409
|
AG | A | 17 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(14): Show | 17 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.557-7190delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035409 | ||||||
| chr2:55035411
|
G | T | 1 | a0001c0001t0005g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.557-7191C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035411 | ||||||
| chr2:55035478
|
TAGAG | T | 4 | a0002c0002t0003g0019a0002c0002t0003g0020a0002c0002t0003g0021others(1): Show | 4 | HG00544.hp2 HG02083.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-7262_557-7259d others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035478 | ||||||
| chr2:55035488
|
T | C | 1 | a0002c0002t0003g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.557-7268A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035488 | ||||||
| chr2:55035529
|
G | A | 10 | a0002c0002t0001g0049a0002c0002t0003g0013a0002c0002t0003g0015others(7): Show | 10 | HG01070.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.557-7309C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035529 | ||||||
| chr2:55035625
|
TA | T | 13 | a0001c0001t0001g0103a0001c0001t0001g0118a0001c0001t0001g0120others(10): Show | 13 | HG01069.hp1 HG01167.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.557-7406delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035625 | ||||||
| chr2:55035656
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.557-7436G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035656 | ||||||
| chr2:55035696
|
T | C | 1 | a0013c0019t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.557-7476A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035696 | ||||||
| chr2:55035727
|
G | C | 1 | a0004c0005t0001g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.557-7507C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035727 | ||||||
| chr2:55035823
|
C | A | 1 | a0004c0005t0001g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.557-7603G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035823 | ||||||
| chr2:55035849
|
T | G | 2 | a0001c0001t0005g0290a0001c0001t0005g0291 | 2 | HG00099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.557-7629A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035849 | ||||||
| chr2:55036007
|
C | T | 128 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.557-7787G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036007 | ||||||
| chr2:55036324
|
G | T | 1 | a0017c0015t0008g0308 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.557-8104C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036324 | ||||||
| chr2:55036471
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.557-8251C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036471 | ||||||
| chr2:55036564
|
T | C | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.557-8344A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036564 | ||||||
| chr2:55036599
|
C | CA | 54 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(51): Show | 55 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.557-8380dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | ||||||
| chr2:55036599
|
C | CAA | 7 | a0001c0001t0001g0118a0001c0001t0001g0263a0001c0001t0002g0292others(4): Show | 7 | HG01109.hp2 HG01175.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.557-8381_557-8380d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | ||||||
| chr2:55036599
|
CA | C | 80 | a0001c0001t0001g0214a0001c0001t0001g0219a0001c0001t0001g0224others(77): Show | 82 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.557-8380delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | ||||||
| chr2:55036599
|
CAA | C | 46 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0087others(43): Show | 46 | HG00099.hp1 HG00741.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.557-8381_557-8380d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | ||||||
| chr2:55036599
|
CAAA | C | 27 | a0001c0001t0001g0086a0001c0001t0005g0011a0001c0001t0005g0277others(24): Show | 30 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.557-8382_557-8380d others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | ||||||
| chr2:55036599
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0010a0001c0001t0001g0227a0001c0001t0001g0228others(3): Show | 7 | NA18951.hp1 NA18971.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.557-8387_557-8380d others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | ||||||
| chr2:55036622
|
AAAT | A | 72 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(69): Show | 79 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.557-8405_557-8403d others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036622 | ||||||
| chr2:55036627
|
A | T | 158 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(155): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.557-8407T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036627 | ||||||
| chr2:55036673
|
T | C | 34 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(31): Show | 37 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.557-8453A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036673 | ||||||
| chr2:55036706
|
G | T | 14 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0002g0190others(11): Show | 14 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.557-8486C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036706 | ||||||
| chr2:55036882
|
A | G | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.557-8662T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036882 | ||||||
| chr2:55036968
|
C | T | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.557-8748G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036968 | ||||||
| chr2:55037139
|
A | G | 12 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261others(9): Show | 14 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-8919T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037139 | ||||||
| chr2:55037197
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.557-8977A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037197 | ||||||
| chr2:55037314
|
T | C | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.557-9094A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037314 | ||||||
| chr2:55037389
|
A | G | 8 | a0001c0001t0002g0190a0001c0001t0007g0332a0001c0001t0007g0333others(5): Show | 8 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-9169T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037389 | ||||||
| chr2:55037430
|
T | C | 4 | a0001c0001t0004g0138a0001c0001t0004g0197a0001c0001t0004g0202others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-9210A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037430 | ||||||
| chr2:55037567
|
T | C | 6 | a0001c0001t0002g0002a0001c0001t0002g0207a0001c0001t0002g0208others(3): Show | 8 | HG00423.hp2 HG00621.hp1 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-9347A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037567 | ||||||
| chr2:55037723
|
C | G | 103 | a0001c0001t0001g0151a0001c0001t0002g0001a0001c0001t0002g0002others(100): Show | 110 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.557-9503G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037723 | ||||||
| chr2:55037823
|
A | C | 3 | a0001c0001t0005g0278a0001c0001t0005g0279a0001c0001t0005g0280 | 3 | HG02647.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.557-9603T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037823 | ||||||
| chr2:55037825
|
G | C | 38 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(35): Show | 41 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.557-9605C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037825 | ||||||
| chr2:55037961
|
T | C | 1 | a0001c0001t0007g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.557-9741A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037961 | ||||||
| chr2:55038062
|
A | C | 1 | a0001c0001t0002g0146 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.557-9842T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038062 | ||||||
| chr2:55038067
|
C | G | 239 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(236): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.557-9847G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038067 | ||||||
| chr2:55038076
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.557-9856A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038076 | ||||||
| chr2:55038332
|
G | A | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.557-10112C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038332 | ||||||
| chr2:55038498
|
C | CAT | 111 | a0001c0001t0001g0151a0001c0001t0002g0001a0001c0001t0002g0002others(108): Show | 120 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.557-10279_557-1027 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038498 | ||||||
| chr2:55038516
|
A | G | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.557-10296T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038516 | ||||||
| chr2:55038649
|
C | T | 138 | a0001c0001t0001g0151a0001c0001t0002g0001a0001c0001t0002g0002others(135): Show | 148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.557-10429G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038649 | ||||||
| chr2:55038688
|
A | G | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.557-10468T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038688 | ||||||
| chr2:55038891
|
C | G | 1 | a0001c0001t0015g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.557-10671G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038891 | ||||||
| chr2:55038900
|
G | T | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.557-10680C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038900 | ||||||
| chr2:55038930
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.557-10710A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038930 | ||||||
| chr2:55038970
|
T | A | 5 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261others(2): Show | 5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-10750A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038970 | ||||||
| chr2:55039052
|
A | G | 1 | a0001c0001t0012g0264 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.556+10693T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039052 | ||||||
| chr2:55039074
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.556+10671A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039074 | ||||||
| chr2:55039384
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.556+10361G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039384 | ||||||
| chr2:55039453
|
AAAAG | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0127 | 3 | HG02559.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.556+10288_556+1029 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039453 | ||||||
| chr2:55039520
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.556+10225G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039520 | ||||||
| chr2:55039535
|
T | G | 7 | a0001c0001t0007g0332a0001c0001t0007g0333a0001c0001t0007g0334others(4): Show | 7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+10210A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039535 | ||||||
| chr2:55039559
|
C | T | 60 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(57): Show | 65 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.556+10186G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039559 | ||||||
| chr2:55039647
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.556+10098A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039647 | ||||||
| chr2:55039819
|
T | C | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+9926A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039819 | ||||||
| chr2:55039881
|
A | T | 1 | a0004c0005t0001g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.556+9864T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039881 | ||||||
| chr2:55040017
|
T | A | 34 | a0001c0001t0005g0011a0001c0001t0005g0278a0001c0001t0005g0279others(31): Show | 37 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.556+9728A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040017 | ||||||
| chr2:55040066
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.556+9679A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040066 | ||||||
| chr2:55040073
|
A | G | 1 | a0001c0001t0005g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.556+9672T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040073 | ||||||
| chr2:55040404
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.556+9341A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040404 | ||||||
| chr2:55040409
|
T | C | 110 | a0001c0001t0001g0151a0001c0001t0002g0001a0001c0001t0002g0002others(107): Show | 119 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.556+9336A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040409 | ||||||
| chr2:55040460
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.556+9285G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040460 | ||||||
| chr2:55040469
|
C | T | 27 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0138others(24): Show | 29 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.556+9276G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040469 | ||||||
| chr2:55040472
|
T | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | NA18987.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.556+9273A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040472 | ||||||
| chr2:55040555
|
G | A | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+9190C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040555 | ||||||
| chr2:55040990
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.556+8755C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040990 | ||||||
| chr2:55041000
|
T | TA | 6 | a0001c0001t0001g0251a0001c0001t0003g0131a0001c0008t0008g0259others(3): Show | 6 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.556+8744dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041000 | ||||||
| chr2:55041000
|
TA | T | 145 | a0001c0001t0001g0151a0001c0001t0001g0214a0001c0001t0001g0252others(142): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.556+8744delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041000 | ||||||
| chr2:55041055
|
G | T | 50 | a0001c0001t0003g0128a0001c0001t0003g0129a0001c0001t0003g0130others(47): Show | 50 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.556+8690C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041055 | ||||||
| chr2:55041080
|
A | AT | 61 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(58): Show | 64 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.556+8664dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041080 | ||||||
| chr2:55041233
|
A | T | 1 | a0001c0001t0005g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.556+8512T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041233 | ||||||
| chr2:55041242
|
T | C | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+8503A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041242 | ||||||
| chr2:55041277
|
G | C | 1 | a0001c0001t0002g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.556+8468C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041277 | ||||||
| chr2:55041334
|
T | G | 1 | a0006c0006t0023g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.556+8411A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041334 | ||||||
| chr2:55041441
|
C | G | 13 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0002g0274others(10): Show | 13 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.556+8304G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041441 | ||||||
| chr2:55041550
|
T | C | 1 | a0001c0001t0002g0185 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.556+8195A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041550 | ||||||
| chr2:55041595
|
G | A | 4 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.556+8150C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041595 | ||||||
| chr2:55041683
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.556+8062T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041683 | ||||||
| chr2:55041716
|
T | G | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+8029A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041716 | ||||||
| chr2:55041902
|
G | T | 13 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0002g0274others(10): Show | 13 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.556+7843C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041902 | ||||||
| chr2:55041917
|
T | G | 1 | a0001c0001t0013g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.556+7828A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041917 | ||||||
| chr2:55042013
|
T | C | 243 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(240): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.556+7732A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042013 | ||||||
| chr2:55042061
|
T | A | 1 | a0005c0004t0002g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.556+7684A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042061 | ||||||
| chr2:55042252
|
A | C | 171 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0086others(168): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.556+7493T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042252 | ||||||
| chr2:55042285
|
A | G | 1 | a0002c0002t0003g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.556+7460T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042285 | ||||||
| chr2:55042546
|
G | A | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.556+7199C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042546 | ||||||
| chr2:55042594
|
G | C | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+7151C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042594 | ||||||
| chr2:55042673
|
G | A | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+7072C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042673 | ||||||
| chr2:55042713
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.556+7032T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042713 | ||||||
| chr2:55042750
|
T | A | 240 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(237): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.556+6995A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042750 | ||||||
| chr2:55042773
|
T | C | 2 | a0005c0004t0002g0009a0005c0004t0002g0137 | 3 | HG01070.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.556+6972A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042773 | ||||||
| chr2:55042812
|
C | T | 130 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(127): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.556+6933G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042812 | ||||||
| chr2:55043016
|
T | C | 1 | a0001c0001t0004g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.556+6729A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043016 | ||||||
| chr2:55043038
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.556+6707T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043038 | ||||||
| chr2:55043071
|
G | A | 1 | a0003c0003t0004g0073 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.556+6674C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043071 | ||||||
| chr2:55043172
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.556+6573G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043172 | ||||||
| chr2:55043187
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.556+6558A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043187 | ||||||
| chr2:55043349
|
T | G | 84 | a0001c0001t0001g0151a0001c0001t0001g0252a0001c0001t0002g0001others(81): Show | 91 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.556+6396A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043349 | ||||||
| chr2:55043493
|
C | T | 83 | a0001c0001t0001g0151a0001c0001t0002g0001a0001c0001t0002g0002others(80): Show | 90 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.556+6252G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043493 | ||||||
| chr2:55043580
|
C | T | 2 | a0001c0001t0004g0138a0001c0001t0004g0197 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.556+6165G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043580 | ||||||
| chr2:55043649
|
A | G | 335 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0074others(332): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.556+6096T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043649 | ||||||
| chr2:55043668
|
C | T | 138 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(135): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.556+6077G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043668 | ||||||
| chr2:55043711
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.556+6034G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043711 | ||||||
| chr2:55043776
|
C | G | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+5969G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043776 | ||||||
| chr2:55043777
|
T | G | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.556+5968A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043777 | ||||||
| chr2:55043839
|
T | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(76): Show | 80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.556+5906A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043839 | ||||||
| chr2:55044052
|
C | T | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+5693G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044052 | ||||||
| chr2:55044057
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.556+5688C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044057 | ||||||
| chr2:55044090
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.556+5655C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044090 | ||||||
| chr2:55044227
|
T | A | 1 | a0004c0005t0001g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.556+5518A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044227 | ||||||
| chr2:55044228
|
T | A | 228 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(225): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.556+5517A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044228 | ||||||
| chr2:55044285
|
G | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0255 | 2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.556+5460C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044285 | ||||||
| chr2:55044399
|
C | G | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.556+5346G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044399 | ||||||
| chr2:55044403
|
C | G | 7 | a0003c0003t0004g0004a0003c0003t0004g0005a0003c0003t0004g0073others(4): Show | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.556+5342G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044403 | ||||||
| chr2:55044407
|
C | G | 1 | a0003c0003t0014g0071 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.556+5338G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044407 | ||||||
| chr2:55044419
|
C | A | 13 | a0001c0001t0004g0077a0001c0001t0004g0138a0001c0001t0004g0139others(10): Show | 13 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.556+5326G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044419 | ||||||
| chr2:55044445
|
T | C | 103 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(100): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.556+5300A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044445 | ||||||
| chr2:55044487
|
G | T | 4 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.556+5258C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044487 | ||||||
| chr2:55044670
|
T | C | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.556+5075A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044670 | ||||||
| chr2:55044683
|
T | C | 1 | a0001c0013t0001g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.556+5062A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044683 | ||||||
| chr2:55044735
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+5010A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044735 | ||||||
| chr2:55044737
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+5008A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044737 | ||||||
| chr2:55044739
|
C | T | 138 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(135): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.556+5006G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044739 | ||||||
| chr2:55044741
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+5004G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044741 | ||||||
| chr2:55044746
|
C | G | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+4999G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044746 | ||||||
| chr2:55044747
|
T | A | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+4998A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044747 | ||||||
| chr2:55044749
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+4996G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044749 | ||||||
| chr2:55044785
|
T | TA | 79 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(76): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.556+4959dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044785 | ||||||
| chr2:55044785
|
T | TAA | 105 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(102): Show | 109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.556+4958_556+4959d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044785 | ||||||
| chr2:55044785
|
T | TAAA | 23 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(20): Show | 23 | HG01123.hp2 HG01346.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.556+4957_556+4959d others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044785 | ||||||
| chr2:55044785
|
TA | T | 34 | a0001c0001t0001g0219a0001c0001t0001g0224a0001c0001t0002g0274others(31): Show | 36 | HG00140.hp1 HG01167.hp1 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.556+4959delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044785 | ||||||
| chr2:55044829
|
C | G | 138 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(135): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.556+4916G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044829 | ||||||
| chr2:55045012
|
T | C | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | NA18952.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.556+4733A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045012 | ||||||
| chr2:55045087
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.556+4658G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045087 | ||||||
| chr2:55045153
|
A | C | 1 | a0001c0001t0001g0223 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.556+4592T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045153 | ||||||
| chr2:55045201
|
A | T | 4 | a0001c0008t0008g0259a0001c0008t0008g0260a0001c0008t0008g0261others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.556+4544T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045201 | ||||||
| chr2:55045295
|
C | T | 1 | a0001c0001t0025g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.556+4450G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045295 | ||||||
| chr2:55045474
|
T | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.556+4271A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045474 | ||||||
| chr2:55045548
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.556+4197A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045548 | ||||||
| chr2:55045905
|
C | T | 2 | a0001c0001t0004g0079a0001c0001t0004g0217 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.556+3840G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045905 | ||||||
| chr2:55046045
|
A | T | 51 | a0001c0001t0005g0011a0001c0001t0005g0277a0001c0001t0005g0278others(48): Show | 56 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.556+3700T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046045 | ||||||
| chr2:55046094
|
GTAAACAG others(6): Show |
G | 6 | a0001c0001t0002g0002a0001c0001t0002g0207a0001c0001t0002g0208others(3): Show | 8 | HG00423.hp2 HG00621.hp1 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.556+3638_556+3650d others(15): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046094 | ||||||
| chr2:55046151
|
C | T | 290 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(287): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.556+3594G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046151 | ||||||
| chr2:55046261
|
A | G | 6 | a0001c0001t0002g0069a0001c0001t0002g0070a0002c0002t0003g0019others(3): Show | 6 | HG00544.hp2 HG02040.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.556+3484T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046261 | ||||||
| chr2:55046357
|
C | T | 10 | a0004c0005t0001g0323a0004c0005t0001g0324a0004c0005t0001g0325others(7): Show | 10 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.556+3388G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046357 | ||||||
| chr2:55046667
|
C | A | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.556+3078G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046667 | ||||||
| chr2:55046747
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.556+2998A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046747 | ||||||
| chr2:55046792
|
T | C | 7 | a0001c0001t0001g0216a0007c0007t0004g0062a0007c0007t0004g0063others(4): Show | 7 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.556+2953A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046792 | ||||||
| chr2:55046836
|
A | C | 1 | a0010c0024t0006g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.556+2909T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046836 | ||||||
| chr2:55046931
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.556+2814A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046931 | ||||||
| chr2:55047161
|
C | G | 1 | a0001c0001t0001g0078 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.556+2584G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047161 | ||||||
| chr2:55047202
|
C | T | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.556+2543G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047202 | ||||||
| chr2:55047266
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.556+2479C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047266 | ||||||
| chr2:55047327
|
C | CA | 7 | a0001c0001t0004g0217a0001c0001t0004g0218a0001c0008t0008g0259others(4): Show | 7 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+2417dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047327 | ||||||
| chr2:55047327
|
CA | C | 82 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0219others(79): Show | 86 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.556+2417delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047327 | ||||||
| chr2:55047327
|
CAA | C | 24 | a0001c0001t0002g0292a0001c0001t0005g0011a0001c0001t0005g0278others(21): Show | 25 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.556+2416_556+2417d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047327 | ||||||
| chr2:55047395
|
C | T | 49 | a0002c0002t0001g0049a0002c0002t0001g0056a0002c0002t0002g0047others(46): Show | 49 | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.556+2350G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047395 | ||||||
| chr2:55047509
|
C | T | 1 | a0001c0001t0017g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.556+2236G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047509 | ||||||
| chr2:55047575
|
GA | G | 293 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075others(290): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.556+2169delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047575 | ||||||
| chr2:55047771
|
T | C | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+1974A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047771 | ||||||
| chr2:55047828
|
C | T | 1 | a0010c0024t0006g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.556+1917G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047828 | ||||||
| chr2:55047881
|
T | A | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1864A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047881 | ||||||
| chr2:55047882
|
G | C | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1863C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047882 | ||||||
| chr2:55047884
|
A | C | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1861T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047884 | ||||||
| chr2:55047886
|
G | C | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1859C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047886 | ||||||
| chr2:55047887
|
A | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1858T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047887 | ||||||
| chr2:55047888
|
A | C | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1857T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047888 | ||||||
| chr2:55047889
|
C | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1856G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047889 | ||||||
| chr2:55047890
|
T | A | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1855A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047890 | ||||||
| chr2:55047892
|
G | C | 51 | a0001c0001t0001g0307a0001c0001t0002g0292a0001c0001t0005g0011others(48): Show | 54 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.556+1853C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047892 | ||||||
| chr2:55047894
|
A | G | 8 | a0001c0008t0018g0067a0003c0003t0004g0004a0003c0003t0004g0005others(5): Show | 10 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.556+1851T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047894 | ||||||
| chr2:55047896
|
A | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1849T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047896 | ||||||
| chr2:55047897
|
C | T | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1848G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047897 | ||||||
| chr2:55047938
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.556+1807C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047938 | ||||||
| chr2:55048192
|
G | A | 11 | a0001c0001t0001g0263a0001c0001t0001g0266a0001c0001t0001g0270others(8): Show | 11 | HG00423.hp1 HG01175.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.556+1553C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048192 | ||||||
| chr2:55048261
|
T | C | 2 | a0001c0001t0006g0309a0001c0001t0006g0310 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.556+1484A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048261 | ||||||
| chr2:55048424
|
G | A | 4 | a0001c0001t0002g0274a0001c0001t0010g0273a0001c0001t0010g0275others(1): Show | 4 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.556+1321C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048424 | ||||||
| chr2:55048476
|
T | A | 38 | a0001c0001t0001g0307a0001c0001t0002g0292a0001c0001t0005g0011others(35): Show | 41 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.556+1269A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048476 | ||||||
| chr2:55048490
|
G | A | 1 | a0001c0001t0002g0311 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.556+1255C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048490 | ||||||
| chr2:55048500
|
A | AT | 56 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0007g0332others(53): Show | 56 | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.556+1244dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048500 | ||||||
| chr2:55048732
|
A | G | 1 | a0004c0005t0001g0323 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.556+1013T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048732 | ||||||
| chr2:55048926
|
C | G | 1 | a0001c0008t0018g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+819G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048926 | ||||||
| chr2:55049070
|
G | A | 1 | a0001c0001t0002g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.556+675C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049070 | ||||||
| chr2:55049086
|
C | A | 1 | a0001c0001t0017g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.556+659G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049086 | ||||||
| chr2:55049094
|
C | T | 5 | a0007c0007t0004g0062a0007c0007t0004g0063a0007c0007t0004g0066others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+651G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049094 | ||||||
| chr2:55049361
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.556+384C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049361 | ||||||
| chr2:55049430
|
C | A | 1 | a0015c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+315G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049430 | ||||||
| chr2:55049522
|
T | C | 1 | a0001c0021t0007g0336 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.556+223A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049522 | ||||||
| chr2:55049558
|
C | T | 5 | a0004c0005t0001g0323a0004c0005t0001g0324a0004c0005t0001g0325others(2): Show | 5 | HG02109.hp1 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+187G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049558 | ||||||
| chr2:55049667
|
G | A | 1 | a0001c0001t0009g0316 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.556+78C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049667 | ||||||
| chr2:55049719
|
G | A | 2 | a0003c0003t0004g0317a0003c0003t0004g0318 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.556+26C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049719 |